Canonical Allele Identifier: CA359802613

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155690C>A (hg19) ; chr5:g.56859863C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859863C>A , CM000667.2:g.56859863C>A	GRCh38
NC_000005.9:g.56155690C>A , CM000667.1:g.56155690C>A	GRCh37
NC_000005.8:g.56191447C>A	NCBI36
NG_031884.1:g.49791C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.782C>A MANE Select	ENSP00000382423.3:p.Thr261Lys
ENST00000399503.3:c.782C>A	ENSP00000382423.3:p.Thr261Lys
NM_005921.1:c.782C>A	NP_005912.1:p.Thr261Lys
XM_005248519.3:c.404C>A	XP_005248576.2:p.Thr135Lys
XM_011543406.1:c.527C>A	XP_011541708.1:p.Thr176Lys
XM_011543407.1:c.782C>A	XP_011541709.1:p.Thr261Lys
XM_011543408.1:c.782C>A	XP_011541710.1:p.Thr261Lys
XM_017009484.1:c.371C>A	XP_016864973.1:p.Thr124Lys
XM_017009485.1:c.293C>A	XP_016864974.1:p.Thr98Lys
XR_001742068.2:n.813C>A
NM_005921.2:c.782C>A MANE Select	NP_005912.1:p.Thr261Lys