Canonical Allele Identifier: CA2578846410
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23166013_23166016del , CM000669.2:g.23166013_23166016del GRCh38
NC_000007.13:g.23205632_23205635del , CM000669.1:g.23205632_23205635del GRCh37
NC_000007.12:g.23172157_23172160del NCBI36
NG_016983.1:g.65280_65283del
NG_016983.2:g.65280_65283del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+75_1177+78del MANE Select ENSP00000343273.4:n.1177+75_1177+78del
ENST00000339077.9:c.1177+75_1177+78del ENSP00000343273.4:n.1177+75_1177+78del
ENST00000409689.5:c.1033+75_1033+78del ENSP00000386263.1:n.1033+75_1033+78del
ENST00000469576.1:n.64+75_64+78del
ENST00000521082.5:c.*1185+75_*1185+78del ENSP00000430351.1:n.*1185+75_*1185+78del
NM_001031710.2:c.1177+75_1177+78del NP_001026880.2:n.1177+75_1177+78del
NM_018846.4:c.1033+75_1033+78del NP_061334.4:n.1033+75_1033+78del
NR_033328.1:n.1601+75_1601+78del
XM_006715753.1:c.1216+75_1216+78del XP_006715816.1:n.1216+75_1216+78del
XM_006715754.1:c.1150+75_1150+78del XP_006715817.1:n.1150+75_1150+78del
XM_006715755.1:c.1150+75_1150+78del XP_006715818.1:n.1150+75_1150+78del
XM_006715756.1:c.1072+75_1072+78del XP_006715819.1:n.1072+75_1072+78del
XM_006715753.3:c.1216+75_1216+78del XP_006715816.1:n.1216+75_1216+78del
XM_006715754.3:c.1150+75_1150+78del XP_006715817.1:n.1150+75_1150+78del
XM_006715755.3:c.1150+75_1150+78del XP_006715818.1:n.1150+75_1150+78del
XM_006715756.3:c.1072+75_1072+78del XP_006715819.1:n.1072+75_1072+78del
XM_017012439.2:c.1111+75_1111+78del XP_016867928.1:n.1111+75_1111+78del
NM_001031710.3:c.1177+75_1177+78del MANE Select NP_001026880.2:n.1177+75_1177+78del
NM_018846.5:c.1033+75_1033+78del NP_061334.4:n.1033+75_1033+78del
NR_033328.2:n.1550+75_1550+78del