Canonical Allele Identifier: CA361048634

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975560C>A (hg19) ; chr5:g.137639871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639871C>A , CM000667.2:g.137639871C>A	GRCh38
NC_000005.9:g.136975560C>A , CM000667.1:g.136975560C>A	GRCh37
NC_000005.8:g.137003459C>A	NCBI36
NG_032569.1:g.101220G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.1010G>T MANE Select	ENSP00000312397.4:p.Arg337Ile
ENST00000309755.8:c.1010G>T	ENSP00000312397.4:p.Arg337Ile
ENST00000502381.1:n.597G>T
ENST00000504208.5:c.*335-11434G>T	ENSP00000423585.1:n.*335-11434G>T
ENST00000505853.1:c.890G>T	ENSP00000426173.1:p.Arg297Ile
ENST00000506491.5:c.764G>T	ENSP00000424828.1:p.Arg255Ile
ENST00000506873.5:n.635G>T
ENST00000508657.5:c.914G>T	ENSP00000422099.1:p.Arg305Ile
NM_001257194.1:c.914G>T	NP_001244123.1:p.Arg305Ile
NM_001257195.1:c.764G>T	NP_001244124.1:p.Arg255Ile
NM_017415.2:c.1010G>T	NP_059111.2:p.Arg337Ile
NM_017415.3:c.1010G>T MANE Select	NP_059111.2:p.Arg337Ile
NM_001257195.2:c.764G>T	NP_001244124.1:p.Arg255Ile