Canonical Allele Identifier: CA1548135361

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56872885C= , CM000667.2:g.56872885C=	GRCh38
NC_000005.9:g.56168712C= , CM000667.1:g.56168712C=	GRCh37
NC_000005.8:g.56204469C=	NCBI36
NG_031884.1:g.62813C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1566C= MANE Select	ENSP00000382423.3:p.Thr522=
ENST00000399503.3:c.1566C=	ENSP00000382423.3:p.Thr522=
NM_005921.1:c.1566C=	NP_005912.1:p.Thr522=
XM_005248519.3:c.1188C=	XP_005248576.2:p.Thr396=
XM_011543406.1:c.1311C=	XP_011541708.1:p.Thr437=
XM_011543407.1:c.1566C=	XP_011541709.1:p.Thr522=
XM_011543408.1:c.1566C=	XP_011541710.1:p.Thr522=
XM_017009484.1:c.1155C=	XP_016864973.1:p.Thr385=
XM_017009485.1:c.1077C=	XP_016864974.1:p.Thr359=
XR_001742068.2:n.1597C=
NM_005921.2:c.1566C= MANE Select	NP_005912.1:p.Thr522=