Canonical Allele Identifier: CA446561024

Gene: KLHL3

Linked Data

• dbSNP Id: rs951676369
• gnomAD v4: 5-137639022-G-T
• MyVariant Identifiers: chr5:g.136974711G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639022G>T , CM000667.2:g.137639022G>T	GRCh38
NC_000005.9:g.136974711G>T , CM000667.1:g.136974711G>T	GRCh37
NC_000005.8:g.137002610G>T	NCBI36
NG_032569.1:g.102069C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1150C>A MANE Select	ENSP00000312397.4:p.Arg384=
ENST00000309755.8:c.1150C>A	ENSP00000312397.4:p.Arg384=
ENST00000502381.1:n.737C>A
ENST00000504208.5:c.*335-10585C>A	ENSP00000423585.1:n.*335-10585C>A
ENST00000505853.1:c.1030C>A	ENSP00000426173.1:p.Arg344=
ENST00000506491.5:c.904C>A	ENSP00000424828.1:p.Arg302=
ENST00000506873.5:n.775C>A
ENST00000508657.5:c.1054C>A	ENSP00000422099.1:p.Arg352=
NM_001257194.1:c.1054C>A	NP_001244123.1:p.Arg352=
NM_001257195.1:c.904C>A	NP_001244124.1:p.Arg302=
NM_017415.2:c.1150C>A	NP_059111.2:p.Arg384=
NM_017415.3:c.1150C>A MANE Select	NP_059111.2:p.Arg384=
NM_001257195.2:c.904C>A	NP_001244124.1:p.Arg302=