Canonical Allele Identifier: CA366981548
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165897C>G , CM000669.2:g.23165897C>G GRCh38
NC_000007.13:g.23205516C>G , CM000669.1:g.23205516C>G GRCh37
NC_000007.12:g.23172041C>G NCBI36
NG_016983.1:g.65164C>G
NG_016983.2:g.65164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1136C>G MANE Select ENSP00000343273.4:p.Ala379Gly
ENST00000339077.9:c.1136C>G ENSP00000343273.4:p.Ala379Gly
ENST00000409689.5:c.992C>G ENSP00000386263.1:p.Ala331Gly
ENST00000469576.1:n.23C>G
ENST00000521082.5:c.*1144C>G ENSP00000430351.1:n.*1144C>G
NM_001031710.2:c.1136C>G NP_001026880.2:p.Ala379Gly
NM_018846.4:c.992C>G NP_061334.4:p.Ala331Gly
NR_033328.1:n.1560C>G
XM_006715753.1:c.1175C>G XP_006715816.1:p.Ala392Gly
XM_006715754.1:c.1109C>G XP_006715817.1:p.Ala370Gly
XM_006715755.1:c.1109C>G XP_006715818.1:p.Ala370Gly
XM_006715756.1:c.1031C>G XP_006715819.1:p.Ala344Gly
XM_006715753.3:c.1175C>G XP_006715816.1:p.Ala392Gly
XM_006715754.3:c.1109C>G XP_006715817.1:p.Ala370Gly
XM_006715755.3:c.1109C>G XP_006715818.1:p.Ala370Gly
XM_006715756.3:c.1031C>G XP_006715819.1:p.Ala344Gly
XM_017012439.2:c.1070C>G XP_016867928.1:p.Ala357Gly
NM_001031710.3:c.1136C>G MANE Select NP_001026880.2:p.Ala379Gly
NM_018846.5:c.992C>G NP_061334.4:p.Ala331Gly
NR_033328.2:n.1509C>G