Canonical Allele Identifier: CA391676930

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40313136G>C (hg19) ; chr15:g.40020935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40020935G>C , CM000677.2:g.40020935G>C	GRCh38
NC_000015.9:g.40313136G>C , CM000677.1:g.40313136G>C	GRCh37
NC_000015.8:g.38100428G>C	NCBI36
NG_034053.1:g.91812G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263791.10:c.4210G>C MANE Select	ENSP00000263791.5:p.Val1404Leu
ENST00000263791.9:c.4210G>C	ENSP00000263791.5:p.Val1404Leu
ENST00000558557.1:n.1202G>C
ENST00000558629.5:n.3127G>C
ENST00000558743.1:n.410G>C
ENST00000560855.5:c.3542G>C
NM_001013703.3:c.4210G>C	NP_001013725.2:p.Val1404Leu
XM_005254392.1:c.4210G>C	XP_005254449.1:p.Val1404Leu
XM_011521599.1:c.4210G>C	XP_011519901.1:p.Val1404Leu
XM_011521600.1:c.4039G>C	XP_011519902.1:p.Val1347Leu
XM_005254392.3:c.4210G>C	XP_005254449.1:p.Val1404Leu
XM_011521599.2:c.4210G>C	XP_011519901.1:p.Val1404Leu
XM_011521600.3:c.4039G>C	XP_011519902.1:p.Val1347Leu
XM_017022219.2:c.4039G>C	XP_016877708.1:p.Val1347Leu
NM_001013703.4:c.4210G>C MANE Select	NP_001013725.2:p.Val1404Leu