Canonical Allele Identifier: CA1585497642

Gene: KLHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639076C= , CM000667.2:g.137639076C=	GRCh38
NC_000005.9:g.136974765C= , CM000667.1:g.136974765C=	GRCh37
NC_000005.8:g.137002664C=	NCBI36
NG_032569.1:g.102015G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1096G= MANE Select	ENSP00000312397.4:p.Val366=
ENST00000309755.8:c.1096G=	ENSP00000312397.4:p.Val366=
ENST00000502381.1:n.683G=
ENST00000504208.5:c.*335-10639G=	ENSP00000423585.1:n.*335-10639G=
ENST00000505853.1:c.976G=	ENSP00000426173.1:p.Val326=
ENST00000506491.5:c.850G=	ENSP00000424828.1:p.Val284=
ENST00000506873.5:n.721G=
ENST00000508657.5:c.1000G=	ENSP00000422099.1:p.Val334=
NM_001257194.1:c.1000G=	NP_001244123.1:p.Val334=
NM_001257195.1:c.850G=	NP_001244124.1:p.Val284=
NM_017415.2:c.1096G=	NP_059111.2:p.Val366=
NM_017415.3:c.1096G= MANE Select	NP_059111.2:p.Val366=
NM_001257195.2:c.850G=	NP_001244124.1:p.Val284=