Canonical Allele Identifier: CA2774715165
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23166072_23166073insACAG , CM000669.2:g.23166072_23166073insACAG GRCh38
NC_000007.13:g.23205691_23205692insACAG , CM000669.1:g.23205691_23205692insACAG GRCh37
NC_000007.12:g.23172216_23172217insACAG NCBI36
NG_016983.1:g.65339_65340insACAG
NG_016983.2:g.65339_65340insACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+134_1177+135insACAG MANE Select ENSP00000343273.4:n.1177+134_1177+135insACAG
ENST00000339077.9:c.1177+134_1177+135insACAG ENSP00000343273.4:n.1177+134_1177+135insACAG
ENST00000409689.5:c.1033+134_1033+135insACAG ENSP00000386263.1:n.1033+134_1033+135insACAG
ENST00000469576.1:n.64+134_64+135insACAG
ENST00000521082.5:c.*1185+134_*1185+135insACAG ENSP00000430351.1:n.*1185+134_*1185+135insACAG
NM_001031710.2:c.1177+134_1177+135insACAG NP_001026880.2:n.1177+134_1177+135insACAG
NM_018846.4:c.1033+134_1033+135insACAG NP_061334.4:n.1033+134_1033+135insACAG
NR_033328.1:n.1601+134_1601+135insACAG
XM_006715753.1:c.1216+134_1216+135insACAG XP_006715816.1:n.1216+134_1216+135insACAG
XM_006715754.1:c.1150+134_1150+135insACAG XP_006715817.1:n.1150+134_1150+135insACAG
XM_006715755.1:c.1150+134_1150+135insACAG XP_006715818.1:n.1150+134_1150+135insACAG
XM_006715756.1:c.1072+134_1072+135insACAG XP_006715819.1:n.1072+134_1072+135insACAG
XM_006715753.3:c.1216+134_1216+135insACAG XP_006715816.1:n.1216+134_1216+135insACAG
XM_006715754.3:c.1150+134_1150+135insACAG XP_006715817.1:n.1150+134_1150+135insACAG
XM_006715755.3:c.1150+134_1150+135insACAG XP_006715818.1:n.1150+134_1150+135insACAG
XM_006715756.3:c.1072+134_1072+135insACAG XP_006715819.1:n.1072+134_1072+135insACAG
XM_017012439.2:c.1111+134_1111+135insACAG XP_016867928.1:n.1111+134_1111+135insACAG
NM_001031710.3:c.1177+134_1177+135insACAG MANE Select NP_001026880.2:n.1177+134_1177+135insACAG
NM_018846.5:c.1033+134_1033+135insACAG NP_061334.4:n.1033+134_1033+135insACAG
NR_033328.2:n.1550+134_1550+135insACAG