Canonical Allele Identifier: CA1548136567

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875522T= , CM000667.2:g.56875522T=	GRCh38
NC_000005.9:g.56171349T= , CM000667.1:g.56171349T=	GRCh37
NC_000005.8:g.56207106T=	NCBI36
NG_031884.1:g.65450T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+212T= MANE Select	ENSP00000382423.3:n.1965+212T=
ENST00000399503.3:c.1965+212T=	ENSP00000382423.3:n.1965+212T=
NM_005921.1:c.1965+212T=	NP_005912.1:n.1965+212T=
XM_005248519.3:c.1587+212T=	XP_005248576.2:n.1587+212T=
XM_011543406.1:c.1710+212T=	XP_011541708.1:n.1710+212T=
XM_011543407.1:c.1686+2517T=	XP_011541709.1:n.1686+2517T=
XM_011543408.1:c.1965+212T=	XP_011541710.1:n.1965+212T=
XM_017009484.1:c.1554+212T=	XP_016864973.1:n.1554+212T=
XM_017009485.1:c.1476+212T=	XP_016864974.1:n.1476+212T=
XR_001742068.2:n.1996+212T=
NM_005921.2:c.1965+212T= MANE Select	NP_005912.1:n.1965+212T=