Canonical Allele Identifier: CA2682028373

Gene: KLHL7

Linked Data

• gnomAD v4: 7-23166002-A-ATATTCAAATAATACCAGCTGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166006_23166007insCAAATAATACCAGCTGTTTATT , CM000669.2:g.23166006_23166007insCAAATAATACCAGCTGTTTATT	GRCh38
NC_000007.13:g.23205625_23205626insCAAATAATACCAGCTGTTTATT , CM000669.1:g.23205625_23205626insCAAATAATACCAGCTGTTTATT	GRCh37
NC_000007.12:g.23172150_23172151insCAAATAATACCAGCTGTTTATT	NCBI36
NG_016983.1:g.65273_65274insCAAATAATACCAGCTGTTTATT
NG_016983.2:g.65273_65274insCAAATAATACCAGCTGTTTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+68_1177+69insCAAATAATACCAGCTGTTTATT MANE Select	ENSP00000343273.4:n.1177+68_1177+69insCAAATAATACCAGCTGTTTATT
ENST00000339077.9:c.1177+68_1177+69insCAAATAATACCAGCTGTTTATT	ENSP00000343273.4:n.1177+68_1177+69insCAAATAATACCAGCTGTTTATT
ENST00000409689.5:c.1033+68_1033+69insCAAATAATACCAGCTGTTTATT	ENSP00000386263.1:n.1033+68_1033+69insCAAATAATACCAGCTGTTTATT
ENST00000469576.1:n.64+68_64+69insCAAATAATACCAGCTGTTTATT
ENST00000521082.5:c.*1185+68_*1185+69insCAAATAATACCAGCTGTTTATT	ENSP00000430351.1:n.*1185+68_*1185+69insCAAATAATACCAGCTGTTTAT...
NM_001031710.2:c.1177+68_1177+69insCAAATAATACCAGCTGTTTATT	NP_001026880.2:n.1177+68_1177+69insCAAATAATACCAGCTGTTTATT
NM_018846.4:c.1033+68_1033+69insCAAATAATACCAGCTGTTTATT	NP_061334.4:n.1033+68_1033+69insCAAATAATACCAGCTGTTTATT
NR_033328.1:n.1601+68_1601+69insCAAATAATACCAGCTGTTTATT
XM_006715753.1:c.1216+68_1216+69insCAAATAATACCAGCTGTTTATT	XP_006715816.1:n.1216+68_1216+69insCAAATAATACCAGCTGTTTATT
XM_006715754.1:c.1150+68_1150+69insCAAATAATACCAGCTGTTTATT	XP_006715817.1:n.1150+68_1150+69insCAAATAATACCAGCTGTTTATT
XM_006715755.1:c.1150+68_1150+69insCAAATAATACCAGCTGTTTATT	XP_006715818.1:n.1150+68_1150+69insCAAATAATACCAGCTGTTTATT
XM_006715756.1:c.1072+68_1072+69insCAAATAATACCAGCTGTTTATT	XP_006715819.1:n.1072+68_1072+69insCAAATAATACCAGCTGTTTATT
XM_006715753.3:c.1216+68_1216+69insCAAATAATACCAGCTGTTTATT	XP_006715816.1:n.1216+68_1216+69insCAAATAATACCAGCTGTTTATT
XM_006715754.3:c.1150+68_1150+69insCAAATAATACCAGCTGTTTATT	XP_006715817.1:n.1150+68_1150+69insCAAATAATACCAGCTGTTTATT
XM_006715755.3:c.1150+68_1150+69insCAAATAATACCAGCTGTTTATT	XP_006715818.1:n.1150+68_1150+69insCAAATAATACCAGCTGTTTATT
XM_006715756.3:c.1072+68_1072+69insCAAATAATACCAGCTGTTTATT	XP_006715819.1:n.1072+68_1072+69insCAAATAATACCAGCTGTTTATT
XM_017012439.2:c.1111+68_1111+69insCAAATAATACCAGCTGTTTATT	XP_016867928.1:n.1111+68_1111+69insCAAATAATACCAGCTGTTTATT
NM_001031710.3:c.1177+68_1177+69insCAAATAATACCAGCTGTTTATT MANE Select	NP_001026880.2:n.1177+68_1177+69insCAAATAATACCAGCTGTTTATT
NM_018846.5:c.1033+68_1033+69insCAAATAATACCAGCTGTTTATT	NP_061334.4:n.1033+68_1033+69insCAAATAATACCAGCTGTTTATT
NR_033328.2:n.1550+68_1550+69insCAAATAATACCAGCTGTTTATT