Canonical Allele Identifier: CA347591659

Gene: EIF2AK3

Linked Data

• gnomAD v4: 2-88575103-G-T
• MyVariant Identifiers: chr2:g.88874621G>T (hg19) ; chr2:g.88575103G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575103G>T , CM000664.2:g.88575103G>T	GRCh38
NC_000002.11:g.88874621G>T , CM000664.1:g.88874621G>T	GRCh37
NC_000002.10:g.88655736G>T	NCBI36
NG_016424.1:g.57474C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2208C>A
ENST00000682276.1:n.1825C>A
ENST00000682892.1:c.1927C>A	ENSP00000507214.1:p.Pro643Thr
ENST00000682952.1:n.2019C>A
ENST00000684455.1:c.1593C>A
ENST00000684642.1:c.1777C>A	ENSP00000507355.1:p.Pro593Thr
ENST00000684740.1:n.2558C>A
ENST00000303236.9:c.2380C>A MANE Select	ENSP00000307235.3:p.Pro794Thr
ENST00000652099.1:c.2574C>A
ENST00000652736.1:n.2256C>A
ENST00000303236.7:c.2380C>A	ENSP00000307235.3:p.Pro794Thr
ENST00000415570.1:c.2017C>A	ENSP00000412076.1:p.Pro673Thr
ENST00000419748.5:c.1927C>A	ENSP00000408325.1:p.Pro643Thr
ENST00000470706.1:n.49-26C>A
NM_001313915.1:c.1927C>A	NP_001300844.1:p.Pro643Thr
NM_004836.5:c.2380C>A	NP_004827.4:p.Pro794Thr
NM_004836.6:c.2380C>A	NP_004827.4:p.Pro794Thr
NR_110236.1:n.1240G>T
XM_005264649.3:c.1696C>A	XP_005264706.1:p.Pro566Thr
XM_017005376.2:c.1696C>A	XP_016860865.1:p.Pro566Thr
NM_004836.7:c.2380C>A MANE Select	NP_004827.4:p.Pro794Thr
NM_001313915.2:c.1927C>A	NP_001300844.1:p.Pro643Thr