Canonical Allele Identifier: CA1548139547

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882301C= , CM000667.2:g.56882301C=	GRCh38
NC_000005.9:g.56178128C= , CM000667.1:g.56178128C=	GRCh37
NC_000005.8:g.56213885C=	NCBI36
NG_031884.1:g.72229C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3101C= MANE Select	ENSP00000382423.3:p.Pro1034=
ENST00000399503.3:c.3101C=	ENSP00000382423.3:p.Pro1034=
NM_005921.1:c.3101C=	NP_005912.1:p.Pro1034=
XM_005248519.3:c.2723C=	XP_005248576.2:p.Pro908=
XM_011543406.1:c.2846C=	XP_011541708.1:p.Pro949=
XM_011543407.1:c.2822C=	XP_011541709.1:p.Pro941=
XM_011543408.1:c.3101C=	XP_011541710.1:p.Pro1034=
XM_017009484.1:c.2690C=	XP_016864973.1:p.Pro897=
XM_017009485.1:c.2612C=	XP_016864974.1:p.Pro871=
XR_001742068.2:n.3132C=
NM_005921.2:c.3101C= MANE Select	NP_005912.1:p.Pro1034=