Canonical Allele Identifier: CA359786300

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177693T>A (hg19) ; chr5:g.56881866T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881866T>A , CM000667.2:g.56881866T>A	GRCh38
NC_000005.9:g.56177693T>A , CM000667.1:g.56177693T>A	GRCh37
NC_000005.8:g.56213450T>A	NCBI36
NG_031884.1:g.71794T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2666T>A MANE Select	ENSP00000382423.3:p.Val889Asp
ENST00000399503.3:c.2666T>A	ENSP00000382423.3:p.Val889Asp
NM_005921.1:c.2666T>A	NP_005912.1:p.Val889Asp
XM_005248519.3:c.2288T>A	XP_005248576.2:p.Val763Asp
XM_011543406.1:c.2411T>A	XP_011541708.1:p.Val804Asp
XM_011543407.1:c.2387T>A	XP_011541709.1:p.Val796Asp
XM_011543408.1:c.2666T>A	XP_011541710.1:p.Val889Asp
XM_017009484.1:c.2255T>A	XP_016864973.1:p.Val752Asp
XM_017009485.1:c.2177T>A	XP_016864974.1:p.Val726Asp
XR_001742068.2:n.2697T>A
NM_005921.2:c.2666T>A MANE Select	NP_005912.1:p.Val889Asp