Canonical Allele Identifier: CA1548129282

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859940G= , CM000667.2:g.56859940G=	GRCh38
NC_000005.9:g.56155767G= , CM000667.1:g.56155767G=	GRCh37
NC_000005.8:g.56191524G=	NCBI36
NG_031884.1:g.49868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+25G= MANE Select	ENSP00000382423.3:n.834+25G=
ENST00000399503.3:c.834+25G=	ENSP00000382423.3:n.834+25G=
NM_005921.1:c.834+25G=	NP_005912.1:n.834+25G=
XM_005248519.3:c.456+25G=	XP_005248576.2:n.456+25G=
XM_011543406.1:c.579+25G=	XP_011541708.1:n.579+25G=
XM_011543407.1:c.834+25G=	XP_011541709.1:n.834+25G=
XM_011543408.1:c.834+25G=	XP_011541710.1:n.834+25G=
XM_017009484.1:c.423+25G=	XP_016864973.1:n.423+25G=
XM_017009485.1:c.345+25G=	XP_016864974.1:n.345+25G=
XR_001742068.2:n.865+25G=
NM_005921.2:c.834+25G= MANE Select	NP_005912.1:n.834+25G=