Canonical Allele Identifier: CA2551163928
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165991_23165992insA , CM000669.2:g.23165991_23165992insA GRCh38
NC_000007.13:g.23205610_23205611insA , CM000669.1:g.23205610_23205611insA GRCh37
NC_000007.12:g.23172135_23172136insA NCBI36
NG_016983.1:g.65258_65259insA
NG_016983.2:g.65258_65259insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+53_1177+54insA MANE Select ENSP00000343273.4:n.1177+53_1177+54insA
ENST00000339077.9:c.1177+53_1177+54insA ENSP00000343273.4:n.1177+53_1177+54insA
ENST00000409689.5:c.1033+53_1033+54insA ENSP00000386263.1:n.1033+53_1033+54insA
ENST00000469576.1:n.64+53_64+54insA
ENST00000521082.5:c.*1185+53_*1185+54insA ENSP00000430351.1:n.*1185+53_*1185+54insA
NM_001031710.2:c.1177+53_1177+54insA NP_001026880.2:n.1177+53_1177+54insA
NM_018846.4:c.1033+53_1033+54insA NP_061334.4:n.1033+53_1033+54insA
NR_033328.1:n.1601+53_1601+54insA
XM_006715753.1:c.1216+53_1216+54insA XP_006715816.1:n.1216+53_1216+54insA
XM_006715754.1:c.1150+53_1150+54insA XP_006715817.1:n.1150+53_1150+54insA
XM_006715755.1:c.1150+53_1150+54insA XP_006715818.1:n.1150+53_1150+54insA
XM_006715756.1:c.1072+53_1072+54insA XP_006715819.1:n.1072+53_1072+54insA
XM_006715753.3:c.1216+53_1216+54insA XP_006715816.1:n.1216+53_1216+54insA
XM_006715754.3:c.1150+53_1150+54insA XP_006715817.1:n.1150+53_1150+54insA
XM_006715755.3:c.1150+53_1150+54insA XP_006715818.1:n.1150+53_1150+54insA
XM_006715756.3:c.1072+53_1072+54insA XP_006715819.1:n.1072+53_1072+54insA
XM_017012439.2:c.1111+53_1111+54insA XP_016867928.1:n.1111+53_1111+54insA
NM_001031710.3:c.1177+53_1177+54insA MANE Select NP_001026880.2:n.1177+53_1177+54insA
NM_018846.5:c.1033+53_1033+54insA NP_061334.4:n.1033+53_1033+54insA
NR_033328.2:n.1550+53_1550+54insA