Canonical Allele Identifier: CA347592516

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874810T>C (hg19) ; chr2:g.88575292T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575292T>C , CM000664.2:g.88575292T>C	GRCh38
NC_000002.11:g.88874810T>C , CM000664.1:g.88874810T>C	GRCh37
NC_000002.10:g.88655925T>C	NCBI36
NG_016424.1:g.57285A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2019A>G
ENST00000682276.1:n.1636A>G
ENST00000682892.1:c.1738A>G	ENSP00000507214.1:p.Thr580Ala
ENST00000682952.1:n.1830A>G
ENST00000684455.1:c.1404A>G
ENST00000684642.1:c.1588A>G	ENSP00000507355.1:p.Thr530Ala
ENST00000684740.1:n.2369A>G
ENST00000303236.9:c.2191A>G MANE Select	ENSP00000307235.3:p.Thr731Ala
ENST00000652099.1:c.2385A>G
ENST00000652736.1:n.2067A>G
ENST00000303236.7:c.2191A>G	ENSP00000307235.3:p.Thr731Ala
ENST00000415570.1:c.1828A>G	ENSP00000412076.1:p.Thr610Ala
ENST00000419748.5:c.1738A>G	ENSP00000408325.1:p.Thr580Ala
ENST00000470706.1:n.48+69A>G
NM_001313915.1:c.1738A>G	NP_001300844.1:p.Thr580Ala
NM_004836.5:c.2191A>G	NP_004827.4:p.Thr731Ala
NM_004836.6:c.2191A>G	NP_004827.4:p.Thr731Ala
NR_110236.1:n.1429T>C
XM_005264649.3:c.1507A>G	XP_005264706.1:p.Thr503Ala
XR_939749.1:n.2470A>G
XM_017005376.2:c.1507A>G	XP_016860865.1:p.Thr503Ala
NM_004836.7:c.2191A>G MANE Select	NP_004827.4:p.Thr731Ala
NM_001313915.2:c.1738A>G	NP_001300844.1:p.Thr580Ala