Canonical Allele Identifier: CA2774715117
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23166020_23166021insACA , CM000669.2:g.23166020_23166021insACA GRCh38
NC_000007.13:g.23205639_23205640insACA , CM000669.1:g.23205639_23205640insACA GRCh37
NC_000007.12:g.23172164_23172165insACA NCBI36
NG_016983.1:g.65287_65288insACA
NG_016983.2:g.65287_65288insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+82_1177+83insACA MANE Select ENSP00000343273.4:n.1177+82_1177+83insACA
ENST00000339077.9:c.1177+82_1177+83insACA ENSP00000343273.4:n.1177+82_1177+83insACA
ENST00000409689.5:c.1033+82_1033+83insACA ENSP00000386263.1:n.1033+82_1033+83insACA
ENST00000469576.1:n.64+82_64+83insACA
ENST00000521082.5:c.*1185+82_*1185+83insACA ENSP00000430351.1:n.*1185+82_*1185+83insACA
NM_001031710.2:c.1177+82_1177+83insACA NP_001026880.2:n.1177+82_1177+83insACA
NM_018846.4:c.1033+82_1033+83insACA NP_061334.4:n.1033+82_1033+83insACA
NR_033328.1:n.1601+82_1601+83insACA
XM_006715753.1:c.1216+82_1216+83insACA XP_006715816.1:n.1216+82_1216+83insACA
XM_006715754.1:c.1150+82_1150+83insACA XP_006715817.1:n.1150+82_1150+83insACA
XM_006715755.1:c.1150+82_1150+83insACA XP_006715818.1:n.1150+82_1150+83insACA
XM_006715756.1:c.1072+82_1072+83insACA XP_006715819.1:n.1072+82_1072+83insACA
XM_006715753.3:c.1216+82_1216+83insACA XP_006715816.1:n.1216+82_1216+83insACA
XM_006715754.3:c.1150+82_1150+83insACA XP_006715817.1:n.1150+82_1150+83insACA
XM_006715755.3:c.1150+82_1150+83insACA XP_006715818.1:n.1150+82_1150+83insACA
XM_006715756.3:c.1072+82_1072+83insACA XP_006715819.1:n.1072+82_1072+83insACA
XM_017012439.2:c.1111+82_1111+83insACA XP_016867928.1:n.1111+82_1111+83insACA
NM_001031710.3:c.1177+82_1177+83insACA MANE Select NP_001026880.2:n.1177+82_1177+83insACA
NM_018846.5:c.1033+82_1033+83insACA NP_061334.4:n.1033+82_1033+83insACA
NR_033328.2:n.1550+82_1550+83insACA