Canonical Allele Identifier: CA2578846361
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165655del , CM000669.2:g.23165655del GRCh38
NC_000007.13:g.23205274del , CM000669.1:g.23205274del GRCh37
NC_000007.12:g.23171799del NCBI36
NG_016983.1:g.64922del
NG_016983.2:g.64922del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.937-43del MANE Select ENSP00000343273.4:n.937-43del
ENST00000339077.9:c.937-43del ENSP00000343273.4:n.937-43del
ENST00000409689.5:c.793-43del ENSP00000386263.1:n.793-43del
ENST00000521082.5:c.*945-43del ENSP00000430351.1:n.*945-43del
NM_001031710.2:c.937-43del NP_001026880.2:n.937-43del
NM_018846.4:c.793-43del NP_061334.4:n.793-43del
NR_033328.1:n.1361-43del
XM_006715753.1:c.976-43del XP_006715816.1:n.976-43del
XM_006715754.1:c.910-43del XP_006715817.1:n.910-43del
XM_006715755.1:c.910-43del XP_006715818.1:n.910-43del
XM_006715756.1:c.832-43del XP_006715819.1:n.832-43del
XM_006715753.3:c.976-43del XP_006715816.1:n.976-43del
XM_006715754.3:c.910-43del XP_006715817.1:n.910-43del
XM_006715755.3:c.910-43del XP_006715818.1:n.910-43del
XM_006715756.3:c.832-43del XP_006715819.1:n.832-43del
XM_017012439.2:c.871-43del XP_016867928.1:n.871-43del
NM_001031710.3:c.937-43del MANE Select NP_001026880.2:n.937-43del
NM_018846.5:c.793-43del NP_061334.4:n.793-43del
NR_033328.2:n.1310-43del