Canonical Allele Identifier: CA1548139339

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881865G= , CM000667.2:g.56881865G=	GRCh38
NC_000005.9:g.56177692G= , CM000667.1:g.56177692G=	GRCh37
NC_000005.8:g.56213449G=	NCBI36
NG_031884.1:g.71793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2665G= MANE Select	ENSP00000382423.3:p.Val889=
ENST00000399503.3:c.2665G=	ENSP00000382423.3:p.Val889=
NM_005921.1:c.2665G=	NP_005912.1:p.Val889=
XM_005248519.3:c.2287G=	XP_005248576.2:p.Val763=
XM_011543406.1:c.2410G=	XP_011541708.1:p.Val804=
XM_011543407.1:c.2386G=	XP_011541709.1:p.Val796=
XM_011543408.1:c.2665G=	XP_011541710.1:p.Val889=
XM_017009484.1:c.2254G=	XP_016864973.1:p.Val752=
XM_017009485.1:c.2176G=	XP_016864974.1:p.Val726=
XR_001742068.2:n.2696G=
NM_005921.2:c.2665G= MANE Select	NP_005912.1:p.Val889=