Canonical Allele Identifier: CA347591238

Gene: EIF2AK3

Linked Data

• gnomAD v4: 2-88575012-G-A
• MyVariant Identifiers: chr2:g.88874530G>A (hg19) ; chr2:g.88575012G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575012G>A , CM000664.2:g.88575012G>A	GRCh38
NC_000002.11:g.88874530G>A , CM000664.1:g.88874530G>A	GRCh37
NC_000002.10:g.88655645G>A	NCBI36
NG_016424.1:g.57565C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2299C>T
ENST00000682103.1:c.12C>T
ENST00000682276.1:n.1916C>T
ENST00000682892.1:c.2018C>T	ENSP00000507214.1:p.Thr673Ile
ENST00000682952.1:n.2110C>T
ENST00000684455.1:c.1684C>T
ENST00000684642.1:c.1868C>T	ENSP00000507355.1:p.Thr623Ile
ENST00000684740.1:n.2649C>T
ENST00000303236.9:c.2471C>T MANE Select	ENSP00000307235.3:p.Thr824Ile
ENST00000652099.1:c.2665C>T
ENST00000652736.1:n.2347C>T
ENST00000303236.7:c.2471C>T	ENSP00000307235.3:p.Thr824Ile
ENST00000415570.1:c.2108C>T	ENSP00000412076.1:p.Thr703Ile
ENST00000419748.5:c.2018C>T	ENSP00000408325.1:p.Thr673Ile
ENST00000470706.1:n.114C>T
NM_001313915.1:c.2018C>T	NP_001300844.1:p.Thr673Ile
NM_004836.5:c.2471C>T	NP_004827.4:p.Thr824Ile
NM_004836.6:c.2471C>T	NP_004827.4:p.Thr824Ile
NR_110236.1:n.1149G>A
XM_005264649.3:c.1787C>T	XP_005264706.1:p.Thr596Ile
XM_017005376.2:c.1787C>T	XP_016860865.1:p.Thr596Ile
NM_004836.7:c.2471C>T MANE Select	NP_004827.4:p.Thr824Ile
NM_001313915.2:c.2018C>T	NP_001300844.1:p.Thr673Ile