Canonical Allele Identifier: CA4186538
Gene: KLHL7 HGNC NCBI

Linked Data

dbSNP Id: rs778971230
gnomAD v2: 7-23205367-A-C
gnomAD v4: 7-23165748-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165748A>C , CM000669.2:g.23165748A>C GRCh38
NC_000007.13:g.23205367A>C , CM000669.1:g.23205367A>C GRCh37
NC_000007.12:g.23171892A>C NCBI36
NG_016983.1:g.65015A>C
NG_016983.2:g.65015A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.987A>C MANE Select ENSP00000343273.4:p.Ala329=
ENST00000339077.9:c.987A>C ENSP00000343273.4:p.Ala329=
ENST00000409689.5:c.843A>C ENSP00000386263.1:p.Ala281=
ENST00000521082.5:c.*995A>C ENSP00000430351.1:n.*995A>C
NM_001031710.2:c.987A>C NP_001026880.2:p.Ala329=
NM_018846.4:c.843A>C NP_061334.4:p.Ala281=
NR_033328.1:n.1411A>C
XM_006715753.1:c.1026A>C XP_006715816.1:p.Ala342=
XM_006715754.1:c.960A>C XP_006715817.1:p.Ala320=
XM_006715755.1:c.960A>C XP_006715818.1:p.Ala320=
XM_006715756.1:c.882A>C XP_006715819.1:p.Ala294=
XM_006715753.3:c.1026A>C XP_006715816.1:p.Ala342=
XM_006715754.3:c.960A>C XP_006715817.1:p.Ala320=
XM_006715755.3:c.960A>C XP_006715818.1:p.Ala320=
XM_006715756.3:c.882A>C XP_006715819.1:p.Ala294=
XM_017012439.2:c.921A>C XP_016867928.1:p.Ala307=
NM_001031710.3:c.987A>C MANE Select NP_001026880.2:p.Ala329=
NM_018846.5:c.843A>C NP_061334.4:p.Ala281=
NR_033328.2:n.1360A>C