Canonical Allele Identifier: CA361048610

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975554C>G (hg19) ; chr5:g.137639865C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639865C>G , CM000667.2:g.137639865C>G	GRCh38
NC_000005.9:g.136975554C>G , CM000667.1:g.136975554C>G	GRCh37
NC_000005.8:g.137003453C>G	NCBI36
NG_032569.1:g.101226G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.1016G>C MANE Select	ENSP00000312397.4:p.Arg339Thr
ENST00000309755.8:c.1016G>C	ENSP00000312397.4:p.Arg339Thr
ENST00000502381.1:n.603G>C
ENST00000504208.5:c.*335-11428G>C	ENSP00000423585.1:n.*335-11428G>C
ENST00000505853.1:c.896G>C	ENSP00000426173.1:p.Arg299Thr
ENST00000506491.5:c.770G>C	ENSP00000424828.1:p.Arg257Thr
ENST00000506873.5:n.641G>C
ENST00000508657.5:c.920G>C	ENSP00000422099.1:p.Arg307Thr
NM_001257194.1:c.920G>C	NP_001244123.1:p.Arg307Thr
NM_001257195.1:c.770G>C	NP_001244124.1:p.Arg257Thr
NM_017415.2:c.1016G>C	NP_059111.2:p.Arg339Thr
NM_017415.3:c.1016G>C MANE Select	NP_059111.2:p.Arg339Thr
NM_001257195.2:c.770G>C	NP_001244124.1:p.Arg257Thr