Canonical Allele Identifier: CA804460037

Gene: KLHL3

Linked Data

• dbSNP Id: rs11428340
• MyVariant Identifiers: chr5:g.136975415_136975416insG (hg19) ; chr5:g.137639726_137639727insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639727dup , CM000667.2:g.137639727dup	GRCh38
NC_000005.9:g.136975416dup , CM000667.1:g.136975416dup	GRCh37
NC_000005.8:g.137003315dup	NCBI36
NG_032569.1:g.101364dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1021+133dup MANE Select	ENSP00000312397.4:n.1021+133dup
ENST00000309755.8:c.1021+133dup	ENSP00000312397.4:n.1021+133dup
ENST00000502381.1:n.608+133dup
ENST00000504208.5:c.*335-11290dup	ENSP00000423585.1:n.*335-11290dup
ENST00000505853.1:c.901+133dup	ENSP00000426173.1:n.901+133dup
ENST00000506491.5:c.775+133dup	ENSP00000424828.1:n.775+133dup
ENST00000506873.5:n.646+133dup
ENST00000508657.5:c.925+133dup	ENSP00000422099.1:n.925+133dup
NM_001257194.1:c.925+133dup	NP_001244123.1:n.925+133dup
NM_001257195.1:c.775+133dup	NP_001244124.1:n.775+133dup
NM_017415.2:c.1021+133dup	NP_059111.2:n.1021+133dup
NM_017415.3:c.1021+133dup MANE Select	NP_059111.2:n.1021+133dup
NM_001257195.2:c.775+133dup	NP_001244124.1:n.775+133dup