Canonical Allele Identifier: CA366981182
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165738G>C , CM000669.2:g.23165738G>C GRCh38
NC_000007.13:g.23205357G>C , CM000669.1:g.23205357G>C GRCh37
NC_000007.12:g.23171882G>C NCBI36
NG_016983.1:g.65005G>C
NG_016983.2:g.65005G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.977G>C MANE Select ENSP00000343273.4:p.Arg326Pro
ENST00000339077.9:c.977G>C ENSP00000343273.4:p.Arg326Pro
ENST00000409689.5:c.833G>C ENSP00000386263.1:p.Arg278Pro
ENST00000521082.5:c.*985G>C ENSP00000430351.1:n.*985G>C
NM_001031710.2:c.977G>C NP_001026880.2:p.Arg326Pro
NM_018846.4:c.833G>C NP_061334.4:p.Arg278Pro
NR_033328.1:n.1401G>C
XM_006715753.1:c.1016G>C XP_006715816.1:p.Arg339Pro
XM_006715754.1:c.950G>C XP_006715817.1:p.Arg317Pro
XM_006715755.1:c.950G>C XP_006715818.1:p.Arg317Pro
XM_006715756.1:c.872G>C XP_006715819.1:p.Arg291Pro
XM_006715753.3:c.1016G>C XP_006715816.1:p.Arg339Pro
XM_006715754.3:c.950G>C XP_006715817.1:p.Arg317Pro
XM_006715755.3:c.950G>C XP_006715818.1:p.Arg317Pro
XM_006715756.3:c.872G>C XP_006715819.1:p.Arg291Pro
XM_017012439.2:c.911G>C XP_016867928.1:p.Arg304Pro
NM_001031710.3:c.977G>C MANE Select NP_001026880.2:p.Arg326Pro
NM_018846.5:c.833G>C NP_061334.4:p.Arg278Pro
NR_033328.2:n.1350G>C