Canonical Allele Identifier: CA1585497569

Gene: KLHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639034T= , CM000667.2:g.137639034T=	GRCh38
NC_000005.9:g.136974723T= , CM000667.1:g.136974723T=	GRCh37
NC_000005.8:g.137002622T=	NCBI36
NG_032569.1:g.102057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1138A= MANE Select	ENSP00000312397.4:p.Met380=
ENST00000309755.8:c.1138A=	ENSP00000312397.4:p.Met380=
ENST00000502381.1:n.725A=
ENST00000504208.5:c.*335-10597A=	ENSP00000423585.1:n.*335-10597A=
ENST00000505853.1:c.1018A=	ENSP00000426173.1:p.Met340=
ENST00000506491.5:c.892A=	ENSP00000424828.1:p.Met298=
ENST00000506873.5:n.763A=
ENST00000508657.5:c.1042A=	ENSP00000422099.1:p.Met348=
NM_001257194.1:c.1042A=	NP_001244123.1:p.Met348=
NM_001257195.1:c.892A=	NP_001244124.1:p.Met298=
NM_017415.2:c.1138A=	NP_059111.2:p.Met380=
NM_017415.3:c.1138A= MANE Select	NP_059111.2:p.Met380=
NM_001257195.2:c.892A=	NP_001244124.1:p.Met298=