Canonical Allele Identifier: CA2774715160

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166070_23166071insT , CM000669.2:g.23166070_23166071insT	GRCh38
NC_000007.13:g.23205689_23205690insT , CM000669.1:g.23205689_23205690insT	GRCh37
NC_000007.12:g.23172214_23172215insT	NCBI36
NG_016983.1:g.65337_65338insT
NG_016983.2:g.65337_65338insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+132_1177+133insT MANE Select	ENSP00000343273.4:n.1177+132_1177+133insT
ENST00000339077.9:c.1177+132_1177+133insT	ENSP00000343273.4:n.1177+132_1177+133insT
ENST00000409689.5:c.1033+132_1033+133insT	ENSP00000386263.1:n.1033+132_1033+133insT
ENST00000469576.1:n.64+132_64+133insT
ENST00000521082.5:c.*1185+132_*1185+133insT	ENSP00000430351.1:n.*1185+132_*1185+133insT
NM_001031710.2:c.1177+132_1177+133insT	NP_001026880.2:n.1177+132_1177+133insT
NM_018846.4:c.1033+132_1033+133insT	NP_061334.4:n.1033+132_1033+133insT
NR_033328.1:n.1601+132_1601+133insT
XM_006715753.1:c.1216+132_1216+133insT	XP_006715816.1:n.1216+132_1216+133insT
XM_006715754.1:c.1150+132_1150+133insT	XP_006715817.1:n.1150+132_1150+133insT
XM_006715755.1:c.1150+132_1150+133insT	XP_006715818.1:n.1150+132_1150+133insT
XM_006715756.1:c.1072+132_1072+133insT	XP_006715819.1:n.1072+132_1072+133insT
XM_006715753.3:c.1216+132_1216+133insT	XP_006715816.1:n.1216+132_1216+133insT
XM_006715754.3:c.1150+132_1150+133insT	XP_006715817.1:n.1150+132_1150+133insT
XM_006715755.3:c.1150+132_1150+133insT	XP_006715818.1:n.1150+132_1150+133insT
XM_006715756.3:c.1072+132_1072+133insT	XP_006715819.1:n.1072+132_1072+133insT
XM_017012439.2:c.1111+132_1111+133insT	XP_016867928.1:n.1111+132_1111+133insT
NM_001031710.3:c.1177+132_1177+133insT MANE Select	NP_001026880.2:n.1177+132_1177+133insT
NM_018846.5:c.1033+132_1033+133insT	NP_061334.4:n.1033+132_1033+133insT
NR_033328.2:n.1550+132_1550+133insT