Canonical Allele Identifier: CA1585498059

Gene: KLHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639571G= , CM000667.2:g.137639571G=	GRCh38
NC_000005.9:g.136975260G= , CM000667.1:g.136975260G=	GRCh37
NC_000005.8:g.137003159G=	NCBI36
NG_032569.1:g.101520C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1021+289C= MANE Select	ENSP00000312397.4:n.1021+289C=
ENST00000309755.8:c.1021+289C=	ENSP00000312397.4:n.1021+289C=
ENST00000502381.1:n.608+289C=
ENST00000504208.5:c.*335-11134C=	ENSP00000423585.1:n.*335-11134C=
ENST00000505853.1:c.901+289C=	ENSP00000426173.1:n.901+289C=
ENST00000506491.5:c.775+289C=	ENSP00000424828.1:n.775+289C=
ENST00000506873.5:n.646+289C=
ENST00000508657.5:c.925+289C=	ENSP00000422099.1:n.925+289C=
NM_001257194.1:c.925+289C=	NP_001244123.1:n.925+289C=
NM_001257195.1:c.775+289C=	NP_001244124.1:n.775+289C=
NM_017415.2:c.1021+289C=	NP_059111.2:n.1021+289C=
NM_017415.3:c.1021+289C= MANE Select	NP_059111.2:n.1021+289C=
NM_001257195.2:c.775+289C=	NP_001244124.1:n.775+289C=