Canonical Allele Identifier: CA1548139527

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882268G= , CM000667.2:g.56882268G=	GRCh38
NC_000005.9:g.56178095G= , CM000667.1:g.56178095G=	GRCh37
NC_000005.8:g.56213852G=	NCBI36
NG_031884.1:g.72196G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3068G= MANE Select	ENSP00000382423.3:p.Arg1023=
ENST00000399503.3:c.3068G=	ENSP00000382423.3:p.Arg1023=
NM_005921.1:c.3068G=	NP_005912.1:p.Arg1023=
XM_005248519.3:c.2690G=	XP_005248576.2:p.Arg897=
XM_011543406.1:c.2813G=	XP_011541708.1:p.Arg938=
XM_011543407.1:c.2789G=	XP_011541709.1:p.Arg930=
XM_011543408.1:c.3068G=	XP_011541710.1:p.Arg1023=
XM_017009484.1:c.2657G=	XP_016864973.1:p.Arg886=
XM_017009485.1:c.2579G=	XP_016864974.1:p.Arg860=
XR_001742068.2:n.3099G=
NM_005921.2:c.3068G= MANE Select	NP_005912.1:p.Arg1023=