Canonical Allele Identifier: CA2774715089

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165999_23166000del , CM000669.2:g.23165999_23166000del	GRCh38
NC_000007.13:g.23205618_23205619del , CM000669.1:g.23205618_23205619del	GRCh37
NC_000007.12:g.23172143_23172144del	NCBI36
NG_016983.1:g.65266_65267del
NG_016983.2:g.65266_65267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+61_1177+62del MANE Select	ENSP00000343273.4:n.1177+61_1177+62del
ENST00000339077.9:c.1177+61_1177+62del	ENSP00000343273.4:n.1177+61_1177+62del
ENST00000409689.5:c.1033+61_1033+62del	ENSP00000386263.1:n.1033+61_1033+62del
ENST00000469576.1:n.64+61_64+62del
ENST00000521082.5:c.*1185+61_*1185+62del	ENSP00000430351.1:n.*1185+61_*1185+62del
NM_001031710.2:c.1177+61_1177+62del	NP_001026880.2:n.1177+61_1177+62del
NM_018846.4:c.1033+61_1033+62del	NP_061334.4:n.1033+61_1033+62del
NR_033328.1:n.1601+61_1601+62del
XM_006715753.1:c.1216+61_1216+62del	XP_006715816.1:n.1216+61_1216+62del
XM_006715754.1:c.1150+61_1150+62del	XP_006715817.1:n.1150+61_1150+62del
XM_006715755.1:c.1150+61_1150+62del	XP_006715818.1:n.1150+61_1150+62del
XM_006715756.1:c.1072+61_1072+62del	XP_006715819.1:n.1072+61_1072+62del
XM_006715753.3:c.1216+61_1216+62del	XP_006715816.1:n.1216+61_1216+62del
XM_006715754.3:c.1150+61_1150+62del	XP_006715817.1:n.1150+61_1150+62del
XM_006715755.3:c.1150+61_1150+62del	XP_006715818.1:n.1150+61_1150+62del
XM_006715756.3:c.1072+61_1072+62del	XP_006715819.1:n.1072+61_1072+62del
XM_017012439.2:c.1111+61_1111+62del	XP_016867928.1:n.1111+61_1111+62del
NM_001031710.3:c.1177+61_1177+62del MANE Select	NP_001026880.2:n.1177+61_1177+62del
NM_018846.5:c.1033+61_1033+62del	NP_061334.4:n.1033+61_1033+62del
NR_033328.2:n.1550+61_1550+62del