Canonical Allele Identifier: CA361047812

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974650C>A (hg19) ; chr5:g.137638961C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137638961C>A , CM000667.2:g.137638961C>A	GRCh38
NC_000005.9:g.136974650C>A , CM000667.1:g.136974650C>A	GRCh37
NC_000005.8:g.137002549C>A	NCBI36
NG_032569.1:g.102130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1211G>T MANE Select	ENSP00000312397.4:p.Gly404Val
ENST00000309755.8:c.1211G>T	ENSP00000312397.4:p.Gly404Val
ENST00000502381.1:n.798G>T
ENST00000504208.5:c.*335-10524G>T	ENSP00000423585.1:n.*335-10524G>T
ENST00000505853.1:c.1091G>T	ENSP00000426173.1:p.Gly364Val
ENST00000506491.5:c.965G>T	ENSP00000424828.1:p.Gly322Val
ENST00000506873.5:n.836G>T
ENST00000508657.5:c.1115G>T	ENSP00000422099.1:p.Gly372Val
NM_001257194.1:c.1115G>T	NP_001244123.1:p.Gly372Val
NM_001257195.1:c.965G>T	NP_001244124.1:p.Gly322Val
NM_017415.2:c.1211G>T	NP_059111.2:p.Gly404Val
NM_017415.3:c.1211G>T MANE Select	NP_059111.2:p.Gly404Val
NM_001257195.2:c.965G>T	NP_001244124.1:p.Gly322Val