Canonical Allele Identifier: CA1548129248

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859864A= , CM000667.2:g.56859864A=	GRCh38
NC_000005.9:g.56155691A= , CM000667.1:g.56155691A=	GRCh37
NC_000005.8:g.56191448A=	NCBI36
NG_031884.1:g.49792A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.783A= MANE Select	ENSP00000382423.3:p.Thr261=
ENST00000399503.3:c.783A=	ENSP00000382423.3:p.Thr261=
NM_005921.1:c.783A=	NP_005912.1:p.Thr261=
XM_005248519.3:c.405A=	XP_005248576.2:p.Thr135=
XM_011543406.1:c.528A=	XP_011541708.1:p.Thr176=
XM_011543407.1:c.783A=	XP_011541709.1:p.Thr261=
XM_011543408.1:c.783A=	XP_011541710.1:p.Thr261=
XM_017009484.1:c.372A=	XP_016864973.1:p.Thr124=
XM_017009485.1:c.294A=	XP_016864974.1:p.Thr98=
XR_001742068.2:n.814A=
NM_005921.2:c.783A= MANE Select	NP_005912.1:p.Thr261=