Canonical Allele Identifier: CA1548129208

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859791A= , CM000667.2:g.56859791A=	GRCh38
NC_000005.9:g.56155618A= , CM000667.1:g.56155618A=	GRCh37
NC_000005.8:g.56191375A=	NCBI36
NG_031884.1:g.49719A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.710A= MANE Select	ENSP00000382423.3:p.Gln237=
ENST00000399503.3:c.710A=	ENSP00000382423.3:p.Gln237=
NM_005921.1:c.710A=	NP_005912.1:p.Gln237=
XM_005248519.3:c.332A=	XP_005248576.2:p.Gln111=
XM_011543406.1:c.455A=	XP_011541708.1:p.Gln152=
XM_011543407.1:c.710A=	XP_011541709.1:p.Gln237=
XM_011543408.1:c.710A=	XP_011541710.1:p.Gln237=
XM_017009484.1:c.299A=	XP_016864973.1:p.Gln100=
XM_017009485.1:c.221A=	XP_016864974.1:p.Gln74=
XR_001742068.2:n.741A=
NM_005921.2:c.710A= MANE Select	NP_005912.1:p.Gln237=