Canonical Allele Identifier: CA427173225

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874934T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575416T>C , CM000664.2:g.88575416T>C	GRCh38
NC_000002.11:g.88874934T>C , CM000664.1:g.88874934T>C	GRCh37
NC_000002.10:g.88656049T>C	NCBI36
NG_016424.1:g.57161A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1895A>G
ENST00000682276.1:n.1512A>G
ENST00000682892.1:c.1614A>G	ENSP00000507214.1:p.Pro538=
ENST00000682952.1:n.1706A>G
ENST00000684455.1:c.1280A>G
ENST00000684642.1:c.1464A>G	ENSP00000507355.1:p.Pro488=
ENST00000684740.1:n.2245A>G
ENST00000303236.9:c.2067A>G MANE Select	ENSP00000307235.3:p.Pro689=
ENST00000652099.1:c.2261A>G
ENST00000652736.1:n.1943A>G
ENST00000303236.7:c.2067A>G	ENSP00000307235.3:p.Pro689=
ENST00000415570.1:c.1704A>G	ENSP00000412076.1:p.Pro568=
ENST00000419748.5:c.1614A>G	ENSP00000408325.1:p.Pro538=
ENST00000478003.1:n.633A>G
NM_001313915.1:c.1614A>G	NP_001300844.1:p.Pro538=
NM_004836.5:c.2067A>G	NP_004827.4:p.Pro689=
NM_004836.6:c.2067A>G	NP_004827.4:p.Pro689=
NR_110236.1:n.1553T>C
XM_005264649.3:c.1383A>G	XP_005264706.1:p.Pro461=
XR_939749.1:n.2346A>G
XM_017005376.2:c.1383A>G	XP_016860865.1:p.Pro461=
NM_004836.7:c.2067A>G MANE Select	NP_004827.4:p.Pro689=
NM_001313915.2:c.1614A>G	NP_001300844.1:p.Pro538=