Canonical Allele Identifier: CA1548136517

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875399A= , CM000667.2:g.56875399A=	GRCh38
NC_000005.9:g.56171226A= , CM000667.1:g.56171226A=	GRCh37
NC_000005.8:g.56206983A=	NCBI36
NG_031884.1:g.65327A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+89A= MANE Select	ENSP00000382423.3:n.1965+89A=
ENST00000399503.3:c.1965+89A=	ENSP00000382423.3:n.1965+89A=
NM_005921.1:c.1965+89A=	NP_005912.1:n.1965+89A=
XM_005248519.3:c.1587+89A=	XP_005248576.2:n.1587+89A=
XM_011543406.1:c.1710+89A=	XP_011541708.1:n.1710+89A=
XM_011543407.1:c.1686+2394A=	XP_011541709.1:n.1686+2394A=
XM_011543408.1:c.1965+89A=	XP_011541710.1:n.1965+89A=
XM_017009484.1:c.1554+89A=	XP_016864973.1:n.1554+89A=
XM_017009485.1:c.1476+89A=	XP_016864974.1:n.1476+89A=
XR_001742068.2:n.1996+89A=
NM_005921.2:c.1965+89A= MANE Select	NP_005912.1:n.1965+89A=