Canonical Allele Identifier: CA1548129227

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859829A= , CM000667.2:g.56859829A=	GRCh38
NC_000005.9:g.56155656A= , CM000667.1:g.56155656A=	GRCh37
NC_000005.8:g.56191413A=	NCBI36
NG_031884.1:g.49757A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.748A= MANE Select	ENSP00000382423.3:p.Ser250=
ENST00000399503.3:c.748A=	ENSP00000382423.3:p.Ser250=
NM_005921.1:c.748A=	NP_005912.1:p.Ser250=
XM_005248519.3:c.370A=	XP_005248576.2:p.Ser124=
XM_011543406.1:c.493A=	XP_011541708.1:p.Ser165=
XM_011543407.1:c.748A=	XP_011541709.1:p.Ser250=
XM_011543408.1:c.748A=	XP_011541710.1:p.Ser250=
XM_017009484.1:c.337A=	XP_016864973.1:p.Ser113=
XM_017009485.1:c.259A=	XP_016864974.1:p.Ser87=
XR_001742068.2:n.779A=
NM_005921.2:c.748A= MANE Select	NP_005912.1:p.Ser250=