Canonical Allele Identifier: CA1548139499

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882193C= , CM000667.2:g.56882193C=	GRCh38
NC_000005.9:g.56178020C= , CM000667.1:g.56178020C=	GRCh37
NC_000005.8:g.56213777C=	NCBI36
NG_031884.1:g.72121C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2993C= MANE Select	ENSP00000382423.3:p.Ala998=
ENST00000399503.3:c.2993C=	ENSP00000382423.3:p.Ala998=
NM_005921.1:c.2993C=	NP_005912.1:p.Ala998=
XM_005248519.3:c.2615C=	XP_005248576.2:p.Ala872=
XM_011543406.1:c.2738C=	XP_011541708.1:p.Ala913=
XM_011543407.1:c.2714C=	XP_011541709.1:p.Ala905=
XM_011543408.1:c.2993C=	XP_011541710.1:p.Ala998=
XM_017009484.1:c.2582C=	XP_016864973.1:p.Ala861=
XM_017009485.1:c.2504C=	XP_016864974.1:p.Ala835=
XR_001742068.2:n.3024C=
NM_005921.2:c.2993C= MANE Select	NP_005912.1:p.Ala998=