Canonical Allele Identifier: CA359785988

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177553T>A (hg19) ; chr5:g.56881726T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881726T>A , CM000667.2:g.56881726T>A	GRCh38
NC_000005.9:g.56177553T>A , CM000667.1:g.56177553T>A	GRCh37
NC_000005.8:g.56213310T>A	NCBI36
NG_031884.1:g.71654T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2526T>A MANE Select	ENSP00000382423.3:p.Ser842Arg
ENST00000399503.3:c.2526T>A	ENSP00000382423.3:p.Ser842Arg
NM_005921.1:c.2526T>A	NP_005912.1:p.Ser842Arg
XM_005248519.3:c.2148T>A	XP_005248576.2:p.Ser716Arg
XM_011543406.1:c.2271T>A	XP_011541708.1:p.Ser757Arg
XM_011543407.1:c.2247T>A	XP_011541709.1:p.Ser749Arg
XM_011543408.1:c.2526T>A	XP_011541710.1:p.Ser842Arg
XM_017009484.1:c.2115T>A	XP_016864973.1:p.Ser705Arg
XM_017009485.1:c.2037T>A	XP_016864974.1:p.Ser679Arg
XR_001742068.2:n.2557T>A
NM_005921.2:c.2526T>A MANE Select	NP_005912.1:p.Ser842Arg