NEW
Try the new Transcript table
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.
Genomic
-
NG_032905.1 RefSeqGene
- Range
-
5001..8297
- Download
- GenBank, FASTA, Sequence Viewer (Graphics), LRG_640
mRNA and Protein(s)
-
NM_001195427.2 → NP_001182356.1 serine/arginine-rich splicing factor 2
See identical proteins and their annotated locations for NP_001182356.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in the 3' UTR compared to variant 1. Variants 1 and 2 both encode the same protein.
- Source sequence(s)
-
AC005837
- Consensus CDS
-
CCDS11749.1
- UniProtKB/Swiss-Prot
- B3KWD5, B4DN89, H0YG49, Q01130
- UniProtKB/TrEMBL
-
Q53FN0
- Related
- ENSP00000353089.5, ENST00000359995.10
- Conserved Domains (1) summary
-
- cd12311
Location:16 → 88
- RRM_SRSF2_SRSF8; RNA recognition motif (RRM) found in serine/arginine-rich splicing factor SRSF2, SRSF8 and similar proteins
-
NM_003016.5 → NP_003007.2 serine/arginine-rich splicing factor 2
See identical proteins and their annotated locations for NP_003007.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the longest transcript. Variants 1 and 2 both encode the same protein.
- Source sequence(s)
-
AC005837
- Consensus CDS
-
CCDS11749.1
- UniProtKB/Swiss-Prot
- B3KWD5, B4DN89, H0YG49, Q01130
- UniProtKB/TrEMBL
-
Q53FN0
- Related
- ENSP00000376276.2, ENST00000392485.2
- Conserved Domains (1) summary
-
- cd12311
Location:16 → 88
- RRM_SRSF2_SRSF8; RNA recognition motif (RRM) found in serine/arginine-rich splicing factor SRSF2, SRSF8 and similar proteins
RNA
-
NR_036608.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) differs in the 3' UTR compared to variant 1. Translation of this transcript would result in it being a candidate for nonsense-mediated mRNA decay (NMD), so it is not thought that this transcript encodes a protein.
- Source sequence(s)
-
AC005837
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_000017.11 Reference GRCh38.p14 Primary Assembly
- Range
-
76734115..76737411 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
RNA
-
XR_429913.5 RNA Sequence
-
XR_429914.5 RNA Sequence
-
XR_002958055.2 RNA Sequence
Alternate T2T-CHM13v2.0
Genomic
-
NC_060941.1 Alternate T2T-CHM13v2.0
- Range
-
77631102..77634398 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
RNA
-
XR_008484875.1 RNA Sequence
-
XR_008484876.1 RNA Sequence
-
XR_008484877.1 RNA Sequence