Canonical Allele Identifier: CA1548136468

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875271C= , CM000667.2:g.56875271C=	GRCh38
NC_000005.9:g.56171098C= , CM000667.1:g.56171098C=	GRCh37
NC_000005.8:g.56206855C=	NCBI36
NG_031884.1:g.65199C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1926C= MANE Select	ENSP00000382423.3:p.Val642=
ENST00000399503.3:c.1926C=	ENSP00000382423.3:p.Val642=
NM_005921.1:c.1926C=	NP_005912.1:p.Val642=
XM_005248519.3:c.1548C=	XP_005248576.2:p.Val516=
XM_011543406.1:c.1671C=	XP_011541708.1:p.Val557=
XM_011543407.1:c.1686+2266C=	XP_011541709.1:n.1686+2266C=
XM_011543408.1:c.1926C=	XP_011541710.1:p.Val642=
XM_017009484.1:c.1515C=	XP_016864973.1:p.Val505=
XM_017009485.1:c.1437C=	XP_016864974.1:p.Val479=
XR_001742068.2:n.1957C=
NM_005921.2:c.1926C= MANE Select	NP_005912.1:p.Val642=