Canonical Allele Identifier: CA347591868

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs1331889033
• gnomAD v2: 2-88874666-T-C
• gnomAD v3: 2-88575148-T-C
• gnomAD v4: 2-88575148-T-C
• MyVariant Identifiers: chr2:g.88874666T>C (hg19) ; chr2:g.88575148T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575148T>C , CM000664.2:g.88575148T>C	GRCh38
NC_000002.11:g.88874666T>C , CM000664.1:g.88874666T>C	GRCh37
NC_000002.10:g.88655781T>C	NCBI36
NG_016424.1:g.57429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2163A>G
ENST00000682276.1:n.1780A>G
ENST00000682892.1:c.1882A>G	ENSP00000507214.1:p.Asn628Asp
ENST00000682952.1:n.1974A>G
ENST00000684455.1:c.1548A>G
ENST00000684642.1:c.1732A>G	ENSP00000507355.1:p.Asn578Asp
ENST00000684740.1:n.2513A>G
ENST00000303236.9:c.2335A>G MANE Select	ENSP00000307235.3:p.Asn779Asp
ENST00000652099.1:c.2529A>G
ENST00000652736.1:n.2211A>G
ENST00000303236.7:c.2335A>G	ENSP00000307235.3:p.Asn779Asp
ENST00000415570.1:c.1972A>G	ENSP00000412076.1:p.Asn658Asp
ENST00000419748.5:c.1882A>G	ENSP00000408325.1:p.Asn628Asp
ENST00000470706.1:n.49-71A>G
NM_001313915.1:c.1882A>G	NP_001300844.1:p.Asn628Asp
NM_004836.5:c.2335A>G	NP_004827.4:p.Asn779Asp
NM_004836.6:c.2335A>G	NP_004827.4:p.Asn779Asp
NR_110236.1:n.1285T>C
XM_005264649.3:c.1651A>G	XP_005264706.1:p.Asn551Asp
XM_017005376.2:c.1651A>G	XP_016860865.1:p.Asn551Asp
NM_004836.7:c.2335A>G MANE Select	NP_004827.4:p.Asn779Asp
NM_001313915.2:c.1882A>G	NP_001300844.1:p.Asn628Asp