Canonical Allele Identifier: CA2145358930

Gene: MAP3K9

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70783094C= , CM000676.2:g.70783094C=	GRCh38
NC_000014.8:g.71249811C= , CM000676.1:g.71249811C=	GRCh37
NC_000014.7:g.70319564C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554752.7:c.820+17573G= MANE Select	ENSP00000451612.2:n.820+17573G=
ENST00000381250.8:c.820+17573G=	ENSP00000370649.4:n.820+17573G=
ENST00000553414.5:c.-99+129G=	ENSP00000451038.1:n.-99+129G=
ENST00000554146.1:c.-16+129G=	ENSP00000451921.1:n.-16+129G=
ENST00000554752.6:c.820+17573G=	ENSP00000451612.2:n.820+17573G=
ENST00000555993.6:c.820+17573G=	ENSP00000451263.2:n.820+17573G=
NM_001284230.1:c.820+17573G=	NP_001271159.1:n.820+17573G=
NM_001284231.1:c.-16+129G=	NP_001271160.1:n.-16+129G=
NM_001284232.1:c.-99+129G=	NP_001271161.1:n.-99+129G=
NM_033141.3:c.820+17573G=	NP_149132.2:n.820+17573G=
XM_005267683.3:c.820+17573G=	XP_005267740.1:n.820+17573G=
XM_011536788.1:c.820+17573G=	XP_011535090.1:n.820+17573G=
XM_011536789.1:c.820+17573G=	XP_011535091.1:n.820+17573G=
XM_011536790.1:c.820+17573G=	XP_011535092.1:n.820+17573G=
XM_011536791.1:c.820+17573G=	XP_011535093.1:n.820+17573G=
XM_011536792.1:c.-99+129G=	XP_011535094.1:n.-99+129G=
XM_005267683.5:c.820+17573G=	XP_005267740.1:n.820+17573G=
XM_011536788.3:c.820+17573G=	XP_011535090.1:n.820+17573G=
NM_033141.4:c.820+17573G=	NP_149132.2:n.820+17573G=
NM_001284230.2:c.820+17573G= MANE Select	NP_001271159.1:n.820+17573G=