Canonical Allele Identifier: CA361045607

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964057A>T (hg19) ; chr5:g.137628368A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628368A>T , CM000667.2:g.137628368A>T	GRCh38
NC_000005.9:g.136964057A>T , CM000667.1:g.136964057A>T	GRCh37
NC_000005.8:g.136991956A>T	NCBI36
NG_032569.1:g.112723T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1520T>A MANE Select	ENSP00000312397.4:p.Val507Asp
ENST00000309755.8:c.1520T>A	ENSP00000312397.4:p.Val507Asp
ENST00000447439.6:n.1576T>A
ENST00000504208.5:c.*404T>A	ENSP00000423585.1:n.*404T>A
ENST00000506491.5:c.1274T>A	ENSP00000424828.1:p.Val425Asp
ENST00000506873.5:n.1043T>A
ENST00000508657.5:c.1424T>A	ENSP00000422099.1:p.Val475Asp
ENST00000509694.1:n.313T>A
NM_001257194.1:c.1424T>A	NP_001244123.1:p.Val475Asp
NM_001257195.1:c.1274T>A	NP_001244124.1:p.Val425Asp
NM_017415.2:c.1520T>A	NP_059111.2:p.Val507Asp
NM_017415.3:c.1520T>A MANE Select	NP_059111.2:p.Val507Asp
NM_001257195.2:c.1274T>A	NP_001244124.1:p.Val425Asp