Canonical Allele Identifier: CA1548139349

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881895A= , CM000667.2:g.56881895A=	GRCh38
NC_000005.9:g.56177722A= , CM000667.1:g.56177722A=	GRCh37
NC_000005.8:g.56213479A=	NCBI36
NG_031884.1:g.71823A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2695A= MANE Select	ENSP00000382423.3:p.Asn899=
ENST00000399503.3:c.2695A=	ENSP00000382423.3:p.Asn899=
NM_005921.1:c.2695A=	NP_005912.1:p.Asn899=
XM_005248519.3:c.2317A=	XP_005248576.2:p.Asn773=
XM_011543406.1:c.2440A=	XP_011541708.1:p.Asn814=
XM_011543407.1:c.2416A=	XP_011541709.1:p.Asn806=
XM_011543408.1:c.2695A=	XP_011541710.1:p.Asn899=
XM_017009484.1:c.2284A=	XP_016864973.1:p.Asn762=
XM_017009485.1:c.2206A=	XP_016864974.1:p.Asn736=
XR_001742068.2:n.2726A=
NM_005921.2:c.2695A= MANE Select	NP_005912.1:p.Asn899=