Canonical Allele Identifier: CA361047918

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974698C>T (hg19) ; chr5:g.137639009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639009C>T , CM000667.2:g.137639009C>T	GRCh38
NC_000005.9:g.136974698C>T , CM000667.1:g.136974698C>T	GRCh37
NC_000005.8:g.137002597C>T	NCBI36
NG_032569.1:g.102082G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1163G>A MANE Select	ENSP00000312397.4:p.Gly388Asp
ENST00000309755.8:c.1163G>A	ENSP00000312397.4:p.Gly388Asp
ENST00000502381.1:n.750G>A
ENST00000504208.5:c.*335-10572G>A	ENSP00000423585.1:n.*335-10572G>A
ENST00000505853.1:c.1043G>A	ENSP00000426173.1:p.Gly348Asp
ENST00000506491.5:c.917G>A	ENSP00000424828.1:p.Gly306Asp
ENST00000506873.5:n.788G>A
ENST00000508657.5:c.1067G>A	ENSP00000422099.1:p.Gly356Asp
NM_001257194.1:c.1067G>A	NP_001244123.1:p.Gly356Asp
NM_001257195.1:c.917G>A	NP_001244124.1:p.Gly306Asp
NM_017415.2:c.1163G>A	NP_059111.2:p.Gly388Asp
NM_017415.3:c.1163G>A MANE Select	NP_059111.2:p.Gly388Asp
NM_001257195.2:c.917G>A	NP_001244124.1:p.Gly306Asp