Canonical Allele Identifier: CA1548136434

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875197G= , CM000667.2:g.56875197G=	GRCh38
NC_000005.9:g.56171024G= , CM000667.1:g.56171024G=	GRCh37
NC_000005.8:g.56206781G=	NCBI36
NG_031884.1:g.65125G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1852G= MANE Select	ENSP00000382423.3:p.Ala618=
ENST00000399503.3:c.1852G=	ENSP00000382423.3:p.Ala618=
NM_005921.1:c.1852G=	NP_005912.1:p.Ala618=
XM_005248519.3:c.1474G=	XP_005248576.2:p.Ala492=
XM_011543406.1:c.1597G=	XP_011541708.1:p.Ala533=
XM_011543407.1:c.1686+2192G=	XP_011541709.1:n.1686+2192G=
XM_011543408.1:c.1852G=	XP_011541710.1:p.Ala618=
XM_017009484.1:c.1441G=	XP_016864973.1:p.Ala481=
XM_017009485.1:c.1363G=	XP_016864974.1:p.Ala455=
XR_001742068.2:n.1883G=
NM_005921.2:c.1852G= MANE Select	NP_005912.1:p.Ala618=