Canonical Allele Identifier: CA446561097

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974778C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639089C>A , CM000667.2:g.137639089C>A	GRCh38
NC_000005.9:g.136974778C>A , CM000667.1:g.136974778C>A	GRCh37
NC_000005.8:g.137002677C>A	NCBI36
NG_032569.1:g.102002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1083G>T MANE Select	ENSP00000312397.4:p.Val361=
ENST00000309755.8:c.1083G>T	ENSP00000312397.4:p.Val361=
ENST00000502381.1:n.670G>T
ENST00000504208.5:c.*335-10652G>T	ENSP00000423585.1:n.*335-10652G>T
ENST00000505853.1:c.963G>T	ENSP00000426173.1:p.Val321=
ENST00000506491.5:c.837G>T	ENSP00000424828.1:p.Val279=
ENST00000506873.5:n.708G>T
ENST00000508657.5:c.987G>T	ENSP00000422099.1:p.Val329=
NM_001257194.1:c.987G>T	NP_001244123.1:p.Val329=
NM_001257195.1:c.837G>T	NP_001244124.1:p.Val279=
NM_017415.2:c.1083G>T	NP_059111.2:p.Val361=
NM_017415.3:c.1083G>T MANE Select	NP_059111.2:p.Val361=
NM_001257195.2:c.837G>T	NP_001244124.1:p.Val279=