Canonical Allele Identifier: CA1585498306

Gene: KLHL3

Linked Data

• dbSNP Id: rs1750864962

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639773G>C , CM000667.2:g.137639773G>C	GRCh38
NC_000005.9:g.136975462G>C , CM000667.1:g.136975462G>C	GRCh37
NC_000005.8:g.137003361G>C	NCBI36
NG_032569.1:g.101318C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.1021+87C>G MANE Select	ENSP00000312397.4:n.1021+87C>G
ENST00000309755.8:c.1021+87C>G	ENSP00000312397.4:n.1021+87C>G
ENST00000502381.1:n.608+87C>G
ENST00000504208.5:c.*335-11336C>G	ENSP00000423585.1:n.*335-11336C>G
ENST00000505853.1:c.901+87C>G	ENSP00000426173.1:n.901+87C>G
ENST00000506491.5:c.775+87C>G	ENSP00000424828.1:n.775+87C>G
ENST00000506873.5:n.646+87C>G
ENST00000508657.5:c.925+87C>G	ENSP00000422099.1:n.925+87C>G
NM_001257194.1:c.925+87C>G	NP_001244123.1:n.925+87C>G
NM_001257195.1:c.775+87C>G	NP_001244124.1:n.775+87C>G
NM_017415.2:c.1021+87C>G	NP_059111.2:n.1021+87C>G
NM_017415.3:c.1021+87C>G MANE Select	NP_059111.2:n.1021+87C>G
NM_001257195.2:c.775+87C>G	NP_001244124.1:n.775+87C>G