Canonical Allele Identifier: CA1548128131

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857463A= , CM000667.2:g.56857463A=	GRCh38
NC_000005.9:g.56153290A= , CM000667.1:g.56153290A=	GRCh37
NC_000005.8:g.56189047A=	NCBI36
NG_031884.1:g.47391A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.633+713A= MANE Select	ENSP00000382423.3:n.633+713A=
ENST00000399503.3:c.633+713A=	ENSP00000382423.3:n.633+713A=
NM_005921.1:c.633+713A=	NP_005912.1:n.633+713A=
XM_005248519.3:c.255+713A=	XP_005248576.2:n.255+713A=
XM_011543406.1:c.378+713A=	XP_011541708.1:n.378+713A=
XM_011543407.1:c.633+713A=	XP_011541709.1:n.633+713A=
XM_011543408.1:c.633+713A=	XP_011541710.1:n.633+713A=
XM_017009484.1:c.222+713A=	XP_016864973.1:n.222+713A=
XM_017009485.1:c.144+713A=	XP_016864974.1:n.144+713A=
XR_001742068.2:n.664+713A=
NM_005921.2:c.633+713A= MANE Select	NP_005912.1:n.633+713A=