Canonical Allele Identifier: CA1585511478

Gene: KLHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628443_137628444delinsAG , CM000667.2:g.137628443_137628444delinsAG	GRCh38
NC_000005.9:g.136964132_136964133delinsAG , CM000667.1:g.136964132_136964133delinsAG	GRCh37
NC_000005.8:g.136992031_136992032delinsAG	NCBI36
NG_032569.1:g.112647_112648delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1451-7_1451-6delinsCT MANE Select	ENSP00000312397.4:n.1451-7_1451-6delinsCT
ENST00000309755.8:c.1451-7_1451-6delinsCT	ENSP00000312397.4:n.1451-7_1451-6delinsCT
ENST00000447439.6:n.1500_1501delinsCT
ENST00000504208.5:c.*335-7_*335-6delinsCT	ENSP00000423585.1:n.*335-7_*335-6delinsCT
ENST00000506491.5:c.1205-7_1205-6delinsCT	ENSP00000424828.1:n.1205-7_1205-6delinsCT
ENST00000506873.5:n.974-7_974-6delinsCT
ENST00000508657.5:c.1355-7_1355-6delinsCT	ENSP00000422099.1:n.1355-7_1355-6delinsCT
ENST00000509694.1:n.237_238delinsCT
NM_001257194.1:c.1355-7_1355-6delinsCT	NP_001244123.1:n.1355-7_1355-6delinsCT
NM_001257195.1:c.1205-7_1205-6delinsCT	NP_001244124.1:n.1205-7_1205-6delinsCT
NM_017415.2:c.1451-7_1451-6delinsCT	NP_059111.2:n.1451-7_1451-6delinsCT
NM_017415.3:c.1451-7_1451-6delinsCT MANE Select	NP_059111.2:n.1451-7_1451-6delinsCT
NM_001257195.2:c.1205-7_1205-6delinsCT	NP_001244124.1:n.1205-7_1205-6delinsCT