Canonical Allele Identifier: CA446561170

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974823A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639134A>T , CM000667.2:g.137639134A>T	GRCh38
NC_000005.9:g.136974823A>T , CM000667.1:g.136974823A>T	GRCh37
NC_000005.8:g.137002722A>T	NCBI36
NG_032569.1:g.101957T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1038T>A MANE Select	ENSP00000312397.4:p.Ala346=
ENST00000309755.8:c.1038T>A	ENSP00000312397.4:p.Ala346=
ENST00000502381.1:n.625T>A
ENST00000504208.5:c.*335-10697T>A	ENSP00000423585.1:n.*335-10697T>A
ENST00000505853.1:c.918T>A	ENSP00000426173.1:p.Ala306=
ENST00000506491.5:c.792T>A	ENSP00000424828.1:p.Ala264=
ENST00000506873.5:n.663T>A
ENST00000508657.5:c.942T>A	ENSP00000422099.1:p.Ala314=
NM_001257194.1:c.942T>A	NP_001244123.1:p.Ala314=
NM_001257195.1:c.792T>A	NP_001244124.1:p.Ala264=
NM_017415.2:c.1038T>A	NP_059111.2:p.Ala346=
NM_017415.3:c.1038T>A MANE Select	NP_059111.2:p.Ala346=
NM_001257195.2:c.792T>A	NP_001244124.1:p.Ala264=