Canonical Allele Identifier: CA361048266

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974780C>T (hg19) ; chr5:g.137639091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639091C>T , CM000667.2:g.137639091C>T	GRCh38
NC_000005.9:g.136974780C>T , CM000667.1:g.136974780C>T	GRCh37
NC_000005.8:g.137002679C>T	NCBI36
NG_032569.1:g.102000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1081G>A MANE Select	ENSP00000312397.4:p.Val361Met
ENST00000309755.8:c.1081G>A	ENSP00000312397.4:p.Val361Met
ENST00000502381.1:n.668G>A
ENST00000504208.5:c.*335-10654G>A	ENSP00000423585.1:n.*335-10654G>A
ENST00000505853.1:c.961G>A	ENSP00000426173.1:p.Val321Met
ENST00000506491.5:c.835G>A	ENSP00000424828.1:p.Val279Met
ENST00000506873.5:n.706G>A
ENST00000508657.5:c.985G>A	ENSP00000422099.1:p.Val329Met
NM_001257194.1:c.985G>A	NP_001244123.1:p.Val329Met
NM_001257195.1:c.835G>A	NP_001244124.1:p.Val279Met
NM_017415.2:c.1081G>A	NP_059111.2:p.Val361Met
NM_017415.3:c.1081G>A MANE Select	NP_059111.2:p.Val361Met
NM_001257195.2:c.835G>A	NP_001244124.1:p.Val279Met