Canonical Allele Identifier: CA2675416331

Gene: KLHL3

Linked Data

• gnomAD v4: 5-137628522-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628522C>G , CM000667.2:g.137628522C>G	GRCh38
NC_000005.9:g.136964211C>G , CM000667.1:g.136964211C>G	GRCh37
NC_000005.8:g.136992110C>G	NCBI36
NG_032569.1:g.112569G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1451-85G>C MANE Select	ENSP00000312397.4:n.1451-85G>C
ENST00000309755.8:c.1451-85G>C	ENSP00000312397.4:n.1451-85G>C
ENST00000447439.6:n.1422G>C
ENST00000504208.5:c.*335-85G>C	ENSP00000423585.1:n.*335-85G>C
ENST00000506491.5:c.1205-85G>C	ENSP00000424828.1:n.1205-85G>C
ENST00000506873.5:n.974-85G>C
ENST00000508657.5:c.1355-85G>C	ENSP00000422099.1:n.1355-85G>C
ENST00000509694.1:n.159G>C
NM_001257194.1:c.1355-85G>C	NP_001244123.1:n.1355-85G>C
NM_001257195.1:c.1205-85G>C	NP_001244124.1:n.1205-85G>C
NM_017415.2:c.1451-85G>C	NP_059111.2:n.1451-85G>C
NM_017415.3:c.1451-85G>C MANE Select	NP_059111.2:n.1451-85G>C
NM_001257195.2:c.1205-85G>C	NP_001244124.1:n.1205-85G>C