Canonical Allele Identifier: CA347593945

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88882951G>A (hg19) ; chr2:g.88583433G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583433G>A , CM000664.2:g.88583433G>A	GRCh38
NC_000002.11:g.88882951G>A , CM000664.1:g.88882951G>A	GRCh37
NC_000002.10:g.88664066G>A	NCBI36
NG_016424.1:g.49144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1205C>T
ENST00000682892.1:c.1307C>T	ENSP00000507214.1:p.Ser436Leu
ENST00000682952.1:n.1399C>T
ENST00000684455.1:c.973C>T
ENST00000684642.1:c.1157C>T	ENSP00000507355.1:p.Ser386Leu
ENST00000303236.9:c.1760C>T MANE Select	ENSP00000307235.3:p.Ser587Leu
ENST00000652099.1:c.1954C>T
ENST00000652736.1:n.1636C>T
ENST00000303236.7:c.1760C>T	ENSP00000307235.3:p.Ser587Leu
ENST00000415570.1:c.1397C>T	ENSP00000412076.1:p.Ser466Leu
ENST00000419748.5:c.1307C>T	ENSP00000408325.1:p.Ser436Leu
NM_001313915.1:c.1307C>T	NP_001300844.1:p.Ser436Leu
NM_004836.5:c.1760C>T	NP_004827.4:p.Ser587Leu
NM_004836.6:c.1760C>T	NP_004827.4:p.Ser587Leu
XM_005264649.3:c.1076C>T	XP_005264706.1:p.Ser359Leu
XR_939749.1:n.1969C>T
XM_017005376.2:c.1076C>T	XP_016860865.1:p.Ser359Leu
NM_004836.7:c.1760C>T MANE Select	NP_004827.4:p.Ser587Leu
NM_001313915.2:c.1307C>T	NP_001300844.1:p.Ser436Leu