Canonical Allele Identifier: CA1694330707
Gene: KLHL7 HGNC NCBI

Linked Data

dbSNP Id: rs1784979529

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165596_23165599del , CM000669.2:g.23165596_23165599del GRCh38
NC_000007.13:g.23205215_23205218del , CM000669.1:g.23205215_23205218del GRCh37
NC_000007.12:g.23171740_23171743del NCBI36
NG_016983.1:g.64863_64866del
NG_016983.2:g.64863_64866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.937-102_937-99del MANE Select ENSP00000343273.4:n.937-102_937-99del
ENST00000339077.9:c.937-102_937-99del ENSP00000343273.4:n.937-102_937-99del
ENST00000409689.5:c.793-102_793-99del ENSP00000386263.1:n.793-102_793-99del
ENST00000521082.5:c.*945-102_*945-99del ENSP00000430351.1:n.*945-102_*945-99del
NM_001031710.2:c.937-102_937-99del NP_001026880.2:n.937-102_937-99del
NM_018846.4:c.793-102_793-99del NP_061334.4:n.793-102_793-99del
NR_033328.1:n.1361-102_1361-99del
XM_006715753.1:c.976-102_976-99del XP_006715816.1:n.976-102_976-99del
XM_006715754.1:c.910-102_910-99del XP_006715817.1:n.910-102_910-99del
XM_006715755.1:c.910-102_910-99del XP_006715818.1:n.910-102_910-99del
XM_006715756.1:c.832-102_832-99del XP_006715819.1:n.832-102_832-99del
XM_006715753.3:c.976-102_976-99del XP_006715816.1:n.976-102_976-99del
XM_006715754.3:c.910-102_910-99del XP_006715817.1:n.910-102_910-99del
XM_006715755.3:c.910-102_910-99del XP_006715818.1:n.910-102_910-99del
XM_006715756.3:c.832-102_832-99del XP_006715819.1:n.832-102_832-99del
XM_017012439.2:c.871-102_871-99del XP_016867928.1:n.871-102_871-99del
NM_001031710.3:c.937-102_937-99del MANE Select NP_001026880.2:n.937-102_937-99del
NM_018846.5:c.793-102_793-99del NP_061334.4:n.793-102_793-99del
NR_033328.2:n.1310-102_1310-99del