Canonical Allele Identifier: CA361049015

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975653A>C (hg19) ; chr5:g.137639964A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639964A>C , CM000667.2:g.137639964A>C	GRCh38
NC_000005.9:g.136975653A>C , CM000667.1:g.136975653A>C	GRCh37
NC_000005.8:g.137003552A>C	NCBI36
NG_032569.1:g.101127T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.917T>G MANE Select	ENSP00000312397.4:p.Val306Gly
ENST00000309755.8:c.917T>G	ENSP00000312397.4:p.Val306Gly
ENST00000502381.1:n.504T>G
ENST00000504208.5:c.*335-11527T>G	ENSP00000423585.1:n.*335-11527T>G
ENST00000505853.1:c.797T>G	ENSP00000426173.1:p.Val266Gly
ENST00000506491.5:c.671T>G	ENSP00000424828.1:p.Val224Gly
ENST00000506873.5:n.542T>G
ENST00000508657.5:c.821T>G	ENSP00000422099.1:p.Val274Gly
NM_001257194.1:c.821T>G	NP_001244123.1:p.Val274Gly
NM_001257195.1:c.671T>G	NP_001244124.1:p.Val224Gly
NM_017415.2:c.917T>G	NP_059111.2:p.Val306Gly
NM_017415.3:c.917T>G MANE Select	NP_059111.2:p.Val306Gly
NM_001257195.2:c.671T>G	NP_001244124.1:p.Val224Gly