Canonical Allele Identifier: CA446561570

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975646G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639957G>C , CM000667.2:g.137639957G>C	GRCh38
NC_000005.9:g.136975646G>C , CM000667.1:g.136975646G>C	GRCh37
NC_000005.8:g.137003545G>C	NCBI36
NG_032569.1:g.101134C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.924C>G MANE Select	ENSP00000312397.4:p.Gly308=
ENST00000309755.8:c.924C>G	ENSP00000312397.4:p.Gly308=
ENST00000502381.1:n.511C>G
ENST00000504208.5:c.*335-11520C>G	ENSP00000423585.1:n.*335-11520C>G
ENST00000505853.1:c.804C>G	ENSP00000426173.1:p.Gly268=
ENST00000506491.5:c.678C>G	ENSP00000424828.1:p.Gly226=
ENST00000506873.5:n.549C>G
ENST00000508657.5:c.828C>G	ENSP00000422099.1:p.Gly276=
NM_001257194.1:c.828C>G	NP_001244123.1:p.Gly276=
NM_001257195.1:c.678C>G	NP_001244124.1:p.Gly226=
NM_017415.2:c.924C>G	NP_059111.2:p.Gly308=
NM_017415.3:c.924C>G MANE Select	NP_059111.2:p.Gly308=
NM_001257195.2:c.678C>G	NP_001244124.1:p.Gly226=