Canonical Allele Identifier: CA361047852

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974668G>C (hg19) ; chr5:g.137638979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137638979G>C , CM000667.2:g.137638979G>C	GRCh38
NC_000005.9:g.136974668G>C , CM000667.1:g.136974668G>C	GRCh37
NC_000005.8:g.137002567G>C	NCBI36
NG_032569.1:g.102112C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1193C>G MANE Select	ENSP00000312397.4:p.Ala398Gly
ENST00000309755.8:c.1193C>G	ENSP00000312397.4:p.Ala398Gly
ENST00000502381.1:n.780C>G
ENST00000504208.5:c.*335-10542C>G	ENSP00000423585.1:n.*335-10542C>G
ENST00000505853.1:c.1073C>G	ENSP00000426173.1:p.Ala358Gly
ENST00000506491.5:c.947C>G	ENSP00000424828.1:p.Ala316Gly
ENST00000506873.5:n.818C>G
ENST00000508657.5:c.1097C>G	ENSP00000422099.1:p.Ala366Gly
NM_001257194.1:c.1097C>G	NP_001244123.1:p.Ala366Gly
NM_001257195.1:c.947C>G	NP_001244124.1:p.Ala316Gly
NM_017415.2:c.1193C>G	NP_059111.2:p.Ala398Gly
NM_017415.3:c.1193C>G MANE Select	NP_059111.2:p.Ala398Gly
NM_001257195.2:c.947C>G	NP_001244124.1:p.Ala316Gly