Canonical Allele Identifier: CA1548129299

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859976A= , CM000667.2:g.56859976A=	GRCh38
NC_000005.9:g.56155803A= , CM000667.1:g.56155803A=	GRCh37
NC_000005.8:g.56191560A=	NCBI36
NG_031884.1:g.49904A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+61A= MANE Select	ENSP00000382423.3:n.834+61A=
ENST00000399503.3:c.834+61A=	ENSP00000382423.3:n.834+61A=
NM_005921.1:c.834+61A=	NP_005912.1:n.834+61A=
XM_005248519.3:c.456+61A=	XP_005248576.2:n.456+61A=
XM_011543406.1:c.579+61A=	XP_011541708.1:n.579+61A=
XM_011543407.1:c.834+61A=	XP_011541709.1:n.834+61A=
XM_011543408.1:c.834+61A=	XP_011541710.1:n.834+61A=
XM_017009484.1:c.423+61A=	XP_016864973.1:n.423+61A=
XM_017009485.1:c.345+61A=	XP_016864974.1:n.345+61A=
XR_001742068.2:n.865+61A=
NM_005921.2:c.834+61A= MANE Select	NP_005912.1:n.834+61A=