Canonical Allele Identifier: CA12718401

Gene: EGR3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22692184C>T , CM000670.2:g.22692184C>T	GRCh38
NC_000008.10:g.22549697C>T , CM000670.1:g.22549697C>T	GRCh37
NC_000008.9:g.22605642C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317216.3:c.154+607G>A MANE Select	ENSP00000318057.2:n.154+607G>A
ENST00000317216.2:c.154+607G>A	ENSP00000318057.2:n.154+607G>A
ENST00000518773.1:n.41G>A
ENST00000519492.1:c.207+118G>A	ENSP00000429370.1:n.207+118G>A
ENST00000522910.1:c.40+118G>A	ENSP00000430310.1:n.40+118G>A
ENST00000524088.1:n.219+315G>A
NM_001199880.1:c.40+118G>A	NP_001186809.1:n.40+118G>A
NM_001199881.1:c.-9+315G>A	NP_001186810.1:n.-9+315G>A
NM_004430.2:c.154+607G>A	NP_004421.2:n.154+607G>A
XM_005273425.2:c.-123G>A	XP_005273482.1:n.-123G>A
XM_005273426.2:c.40+118G>A	XP_005273483.1:n.40+118G>A
XM_011544429.1:c.211+118G>A	XP_011542731.1:n.211+118G>A
XM_005273425.3:c.-123G>A	XP_005273482.1:n.-123G>A
XM_005273426.3:c.40+118G>A	XP_005273483.1:n.40+118G>A
XM_011544429.2:c.211+118G>A	XP_011542731.1:n.211+118G>A
NM_004430.3:c.154+607G>A MANE Select	NP_004421.2:n.154+607G>A
NM_001199880.2:c.40+118G>A	NP_001186809.1:n.40+118G>A
NM_001199881.2:c.-9+315G>A	NP_001186810.1:n.-9+315G>A