Canonical Allele Identifier: CA361047895

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974687G>C (hg19) ; chr5:g.137638998G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137638998G>C , CM000667.2:g.137638998G>C	GRCh38
NC_000005.9:g.136974687G>C , CM000667.1:g.136974687G>C	GRCh37
NC_000005.8:g.137002586G>C	NCBI36
NG_032569.1:g.102093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1174C>G MANE Select	ENSP00000312397.4:p.Leu392Val
ENST00000309755.8:c.1174C>G	ENSP00000312397.4:p.Leu392Val
ENST00000502381.1:n.761C>G
ENST00000504208.5:c.*335-10561C>G	ENSP00000423585.1:n.*335-10561C>G
ENST00000505853.1:c.1054C>G	ENSP00000426173.1:p.Leu352Val
ENST00000506491.5:c.928C>G	ENSP00000424828.1:p.Leu310Val
ENST00000506873.5:n.799C>G
ENST00000508657.5:c.1078C>G	ENSP00000422099.1:p.Leu360Val
NM_001257194.1:c.1078C>G	NP_001244123.1:p.Leu360Val
NM_001257195.1:c.928C>G	NP_001244124.1:p.Leu310Val
NM_017415.2:c.1174C>G	NP_059111.2:p.Leu392Val
NM_017415.3:c.1174C>G MANE Select	NP_059111.2:p.Leu392Val
NM_001257195.2:c.928C>G	NP_001244124.1:p.Leu310Val