Canonical Allele Identifier: CA2774715148

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166055_23166056insC , CM000669.2:g.23166055_23166056insC	GRCh38
NC_000007.13:g.23205674_23205675insC , CM000669.1:g.23205674_23205675insC	GRCh37
NC_000007.12:g.23172199_23172200insC	NCBI36
NG_016983.1:g.65322_65323insC
NG_016983.2:g.65322_65323insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+117_1177+118insC MANE Select	ENSP00000343273.4:n.1177+117_1177+118insC
ENST00000339077.9:c.1177+117_1177+118insC	ENSP00000343273.4:n.1177+117_1177+118insC
ENST00000409689.5:c.1033+117_1033+118insC	ENSP00000386263.1:n.1033+117_1033+118insC
ENST00000469576.1:n.64+117_64+118insC
ENST00000521082.5:c.*1185+117_*1185+118insC	ENSP00000430351.1:n.*1185+117_*1185+118insC
NM_001031710.2:c.1177+117_1177+118insC	NP_001026880.2:n.1177+117_1177+118insC
NM_018846.4:c.1033+117_1033+118insC	NP_061334.4:n.1033+117_1033+118insC
NR_033328.1:n.1601+117_1601+118insC
XM_006715753.1:c.1216+117_1216+118insC	XP_006715816.1:n.1216+117_1216+118insC
XM_006715754.1:c.1150+117_1150+118insC	XP_006715817.1:n.1150+117_1150+118insC
XM_006715755.1:c.1150+117_1150+118insC	XP_006715818.1:n.1150+117_1150+118insC
XM_006715756.1:c.1072+117_1072+118insC	XP_006715819.1:n.1072+117_1072+118insC
XM_006715753.3:c.1216+117_1216+118insC	XP_006715816.1:n.1216+117_1216+118insC
XM_006715754.3:c.1150+117_1150+118insC	XP_006715817.1:n.1150+117_1150+118insC
XM_006715755.3:c.1150+117_1150+118insC	XP_006715818.1:n.1150+117_1150+118insC
XM_006715756.3:c.1072+117_1072+118insC	XP_006715819.1:n.1072+117_1072+118insC
XM_017012439.2:c.1111+117_1111+118insC	XP_016867928.1:n.1111+117_1111+118insC
NM_001031710.3:c.1177+117_1177+118insC MANE Select	NP_001026880.2:n.1177+117_1177+118insC
NM_018846.5:c.1033+117_1033+118insC	NP_061334.4:n.1033+117_1033+118insC
NR_033328.2:n.1550+117_1550+118insC