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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_001035254.3 → NP_001030331.1 early estrogen-induced gene 1 protein isoform a
See identical proteins and their annotated locations for NP_001030331.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (a).
- Source sequence(s)
-
AK058004, AL157935, BC047949, BI008660, CN482844
- Consensus CDS
-
CCDS35150.1
- UniProtKB/Swiss-Prot
- A2A329, Q5T9C2, Q8TEL4
- Related
- ENSP00000362187.1, ENST00000373095.6
- Conserved Domains (1) summary
-
- pfam10358
Location:12 → 152
- NT-C2; N-terminal C2 in EEIG1 and EHBP1 proteins
-
NM_203305.3 → NP_976050.1 early estrogen-induced gene 1 protein isoform b
See identical proteins and their annotated locations for NP_976050.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR and coding region compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a.
- Source sequence(s)
-
AL157935, BC047949, BI008660
- Consensus CDS
-
CCDS6888.1
- UniProtKB/Swiss-Prot
-
Q5T9C2
- Related
- ENSP00000362176.4, ENST00000373084.8
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_000009.12 Reference GRCh38.p14 Primary Assembly
- Range
-
127940582..127980989 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060933.1 Alternate T2T-CHM13v2.0
- Range
-
140148362..140188761 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)