Canonical Allele Identifier: CA361045591

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964053C>G (hg19) ; chr5:g.137628364C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628364C>G , CM000667.2:g.137628364C>G	GRCh38
NC_000005.9:g.136964053C>G , CM000667.1:g.136964053C>G	GRCh37
NC_000005.8:g.136991952C>G	NCBI36
NG_032569.1:g.112727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1524G>C MANE Select	ENSP00000312397.4:p.Glu508Asp
ENST00000309755.8:c.1524G>C	ENSP00000312397.4:p.Glu508Asp
ENST00000447439.6:n.1580G>C
ENST00000504208.5:c.*408G>C	ENSP00000423585.1:n.*408G>C
ENST00000506491.5:c.1278G>C	ENSP00000424828.1:p.Glu426Asp
ENST00000506873.5:n.1047G>C
ENST00000508657.5:c.1428G>C	ENSP00000422099.1:p.Glu476Asp
ENST00000509694.1:n.317G>C
NM_001257194.1:c.1428G>C	NP_001244123.1:p.Glu476Asp
NM_001257195.1:c.1278G>C	NP_001244124.1:p.Glu426Asp
NM_017415.2:c.1524G>C	NP_059111.2:p.Glu508Asp
NM_017415.3:c.1524G>C MANE Select	NP_059111.2:p.Glu508Asp
NM_001257195.2:c.1278G>C	NP_001244124.1:p.Glu426Asp