Canonical Allele Identifier: CA128097117

Gene: KLHL3

Linked Data

• dbSNP Id: rs953386950
• gnomAD v3: 5-137628247-G-C
• gnomAD v4: 5-137628247-G-C
• MyVariant Identifiers: chr5:g.136963936G>C (hg19) ; chr5:g.137628247G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628247G>C , CM000667.2:g.137628247G>C	GRCh38
NC_000005.9:g.136963936G>C , CM000667.1:g.136963936G>C	GRCh37
NC_000005.8:g.136991835G>C	NCBI36
NG_032569.1:g.112844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1591+50C>G MANE Select	ENSP00000312397.4:n.1591+50C>G
ENST00000309755.8:c.1591+50C>G	ENSP00000312397.4:n.1591+50C>G
ENST00000447439.6:n.1647+50C>G
ENST00000504208.5:c.*475+50C>G	ENSP00000423585.1:n.*475+50C>G
ENST00000506491.5:c.1345+50C>G	ENSP00000424828.1:n.1345+50C>G
ENST00000506873.5:n.1114+50C>G
ENST00000508657.5:c.1495+50C>G	ENSP00000422099.1:n.1495+50C>G
ENST00000509694.1:n.434C>G
NM_001257194.1:c.1495+50C>G	NP_001244123.1:n.1495+50C>G
NM_001257195.1:c.1345+50C>G	NP_001244124.1:n.1345+50C>G
NM_017415.2:c.1591+50C>G	NP_059111.2:n.1591+50C>G
NM_017415.3:c.1591+50C>G MANE Select	NP_059111.2:n.1591+50C>G
NM_001257195.2:c.1345+50C>G	NP_001244124.1:n.1345+50C>G