Canonical Allele Identifier: CA804459801

Gene: KLHL3

Linked Data

• dbSNP Id: rs1470208028
• gnomAD v3: 5-137639206-T-C
• gnomAD v4: 5-137639206-T-C
• MyVariant Identifiers: chr5:g.136974895T>C (hg19) ; chr5:g.137639206T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639206T>C , CM000667.2:g.137639206T>C	GRCh38
NC_000005.9:g.136974895T>C , CM000667.1:g.136974895T>C	GRCh37
NC_000005.8:g.137002794T>C	NCBI36
NG_032569.1:g.101885A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1022-56A>G MANE Select	ENSP00000312397.4:n.1022-56A>G
ENST00000309755.8:c.1022-56A>G	ENSP00000312397.4:n.1022-56A>G
ENST00000502381.1:n.609-56A>G
ENST00000504208.5:c.*335-10769A>G	ENSP00000423585.1:n.*335-10769A>G
ENST00000505853.1:c.902-56A>G	ENSP00000426173.1:n.902-56A>G
ENST00000506491.5:c.776-56A>G	ENSP00000424828.1:n.776-56A>G
ENST00000506873.5:n.647-56A>G
ENST00000508657.5:c.926-56A>G	ENSP00000422099.1:n.926-56A>G
NM_001257194.1:c.926-56A>G	NP_001244123.1:n.926-56A>G
NM_001257195.1:c.776-56A>G	NP_001244124.1:n.776-56A>G
NM_017415.2:c.1022-56A>G	NP_059111.2:n.1022-56A>G
NM_017415.3:c.1022-56A>G MANE Select	NP_059111.2:n.1022-56A>G
NM_001257195.2:c.776-56A>G	NP_001244124.1:n.776-56A>G