Canonical Allele Identifier: CA1548139341

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881872A= , CM000667.2:g.56881872A=	GRCh38
NC_000005.9:g.56177699A= , CM000667.1:g.56177699A=	GRCh37
NC_000005.8:g.56213456A=	NCBI36
NG_031884.1:g.71800A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2672A= MANE Select	ENSP00000382423.3:p.Asn891=
ENST00000399503.3:c.2672A=	ENSP00000382423.3:p.Asn891=
NM_005921.1:c.2672A=	NP_005912.1:p.Asn891=
XM_005248519.3:c.2294A=	XP_005248576.2:p.Asn765=
XM_011543406.1:c.2417A=	XP_011541708.1:p.Asn806=
XM_011543407.1:c.2393A=	XP_011541709.1:p.Asn798=
XM_011543408.1:c.2672A=	XP_011541710.1:p.Asn891=
XM_017009484.1:c.2261A=	XP_016864973.1:p.Asn754=
XM_017009485.1:c.2183A=	XP_016864974.1:p.Asn728=
XR_001742068.2:n.2703A=
NM_005921.2:c.2672A= MANE Select	NP_005912.1:p.Asn891=