Canonical Allele Identifier: CA361045582

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964051A>T (hg19) ; chr5:g.137628362A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628362A>T , CM000667.2:g.137628362A>T	GRCh38
NC_000005.9:g.136964051A>T , CM000667.1:g.136964051A>T	GRCh37
NC_000005.8:g.136991950A>T	NCBI36
NG_032569.1:g.112729T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1526T>A MANE Select	ENSP00000312397.4:p.Val509Asp
ENST00000309755.8:c.1526T>A	ENSP00000312397.4:p.Val509Asp
ENST00000447439.6:n.1582T>A
ENST00000504208.5:c.*410T>A	ENSP00000423585.1:n.*410T>A
ENST00000506491.5:c.1280T>A	ENSP00000424828.1:p.Val427Asp
ENST00000506873.5:n.1049T>A
ENST00000508657.5:c.1430T>A	ENSP00000422099.1:p.Val477Asp
ENST00000509694.1:n.319T>A
NM_001257194.1:c.1430T>A	NP_001244123.1:p.Val477Asp
NM_001257195.1:c.1280T>A	NP_001244124.1:p.Val427Asp
NM_017415.2:c.1526T>A	NP_059111.2:p.Val509Asp
NM_017415.3:c.1526T>A MANE Select	NP_059111.2:p.Val509Asp
NM_001257195.2:c.1280T>A	NP_001244124.1:p.Val427Asp