Canonical Allele Identifier: CA361048988

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975645G>T (hg19) ; chr5:g.137639956G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639956G>T , CM000667.2:g.137639956G>T	GRCh38
NC_000005.9:g.136975645G>T , CM000667.1:g.136975645G>T	GRCh37
NC_000005.8:g.137003544G>T	NCBI36
NG_032569.1:g.101135C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.925C>A MANE Select	ENSP00000312397.4:p.Gln309Lys
ENST00000309755.8:c.925C>A	ENSP00000312397.4:p.Gln309Lys
ENST00000502381.1:n.512C>A
ENST00000504208.5:c.*335-11519C>A	ENSP00000423585.1:n.*335-11519C>A
ENST00000505853.1:c.805C>A	ENSP00000426173.1:p.Gln269Lys
ENST00000506491.5:c.679C>A	ENSP00000424828.1:p.Gln227Lys
ENST00000506873.5:n.550C>A
ENST00000508657.5:c.829C>A	ENSP00000422099.1:p.Gln277Lys
NM_001257194.1:c.829C>A	NP_001244123.1:p.Gln277Lys
NM_001257195.1:c.679C>A	NP_001244124.1:p.Gln227Lys
NM_017415.2:c.925C>A	NP_059111.2:p.Gln309Lys
NM_017415.3:c.925C>A MANE Select	NP_059111.2:p.Gln309Lys
NM_001257195.2:c.679C>A	NP_001244124.1:p.Gln227Lys