Canonical Allele Identifier: CA361047879

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974680T>A (hg19) ; chr5:g.137638991T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137638991T>A , CM000667.2:g.137638991T>A	GRCh38
NC_000005.9:g.136974680T>A , CM000667.1:g.136974680T>A	GRCh37
NC_000005.8:g.137002579T>A	NCBI36
NG_032569.1:g.102100A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1181A>T MANE Select	ENSP00000312397.4:p.Asp394Val
ENST00000309755.8:c.1181A>T	ENSP00000312397.4:p.Asp394Val
ENST00000502381.1:n.768A>T
ENST00000504208.5:c.*335-10554A>T	ENSP00000423585.1:n.*335-10554A>T
ENST00000505853.1:c.1061A>T	ENSP00000426173.1:p.Asp354Val
ENST00000506491.5:c.935A>T	ENSP00000424828.1:p.Asp312Val
ENST00000506873.5:n.806A>T
ENST00000508657.5:c.1085A>T	ENSP00000422099.1:p.Asp362Val
NM_001257194.1:c.1085A>T	NP_001244123.1:p.Asp362Val
NM_001257195.1:c.935A>T	NP_001244124.1:p.Asp312Val
NM_017415.2:c.1181A>T	NP_059111.2:p.Asp394Val
NM_017415.3:c.1181A>T MANE Select	NP_059111.2:p.Asp394Val
NM_001257195.2:c.935A>T	NP_001244124.1:p.Asp312Val