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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001318767.2 → NP_001305696.1 large ribosomal subunit protein uL14m isoform a precursor
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) uses an alternate splice sites in the 5' UTR compared to variant 1. Variants 1, 2, and 3 encode the same isoform (a).
- Source sequence(s)
-
AA887574, AL109615, BM013002, BU597168
- Consensus CDS
-
CCDS34460.1
- UniProtKB/Swiss-Prot
- B2R575, Q6P1L8, Q96Q72
- Conserved Domains (1) summary
-
- cl00328
Location:33 → 141
- Ribosomal_L14; Ribosomal protein L14p/L23e
-
NM_001318768.2 → NP_001305697.1 large ribosomal subunit protein uL14m isoform a precursor
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1, 2, and 3 encode the same isoform (a).
- Source sequence(s)
-
AA887574, AL109615, AL365192, BM013002, CK823336
- Consensus CDS
-
CCDS34460.1
- UniProtKB/Swiss-Prot
- B2R575, Q6P1L8, Q96Q72
- Conserved Domains (1) summary
-
- cl00328
Location:33 → 141
- Ribosomal_L14; Ribosomal protein L14p/L23e
-
NM_001318769.2 → NP_001305698.1 large ribosomal subunit protein uL14m isoform b
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) differs in the 5' UTR and initiates translation at an alternate start codon compared to variant 1. The encoded isoform (b) has a longer N-terminus than isoform a.
- Source sequence(s)
-
AA887574, AL109615, AL365192, BM013002, CF541260
- Conserved Domains (1) summary
-
- cl00328
Location:43 → 153
- Ribosomal_L14; Ribosomal protein L14p/L23e
-
NM_001318770.2 → NP_001305699.1 large ribosomal subunit protein uL14m isoform c
Status: REVIEWED
- Description
- Transcript Variant: This variant (5) differs in the 5' UTR and initiates translation at an alternate start codon compared to variant 1. The encoded isoform (c) has a longer N-terminus than isoform a.
- Source sequence(s)
-
AA887574, AL109615, AL365192, BG545603, BM013002
- Conserved Domains (1) summary
-
- cl00328
Location:85 → 195
- Ribosomal_L14; Ribosomal protein L14p/L23e
-
NM_001318771.2 → NP_001305700.1 large ribosomal subunit protein uL14m isoform d
Status: REVIEWED
- Description
- Transcript Variant: This variant (6) lacks an exon in the 5' region and initiates translation at a downstream start codon compared to variant 1. The encoded isoform (d) has a shorter N-terminus than isoform a.
- Source sequence(s)
-
AA887574, AL109615, BM013002, BM559405, BU753526
- Conserved Domains (1) summary
-
- cl00328
Location:2 → 108
- Ribosomal_L14; Ribosomal protein L14p/L23e
-
NM_032111.4 → NP_115487.2 large ribosomal subunit protein uL14m isoform a precursor
See identical proteins and their annotated locations for NP_115487.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes isoform a. Variants 1, 2, and 3 encode the same isoform (a).
- Source sequence(s)
-
AA887574, AL109615, BM559405
- Consensus CDS
-
CCDS34460.1
- UniProtKB/Swiss-Prot
- B2R575, Q6P1L8, Q96Q72
- Related
- ENSP00000361084.3, ENST00000372014.5
- Conserved Domains (1) summary
-
- cl00328
Location:33 → 141
- Ribosomal_L14; Ribosomal protein L14p/L23e
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000006.12 Reference GRCh38.p14 Primary Assembly
- Range
-
44113451..44127452 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060930.1 Alternate T2T-CHM13v2.0
- Range
-
43946908..43960908 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)