Canonical Allele Identifier: CA2774715141

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166047_23166053del , CM000669.2:g.23166047_23166053del	GRCh38
NC_000007.13:g.23205666_23205672del , CM000669.1:g.23205666_23205672del	GRCh37
NC_000007.12:g.23172191_23172197del	NCBI36
NG_016983.1:g.65314_65320del
NG_016983.2:g.65314_65320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+109_1177+115del MANE Select	ENSP00000343273.4:n.1177+109_1177+115del
ENST00000339077.9:c.1177+109_1177+115del	ENSP00000343273.4:n.1177+109_1177+115del
ENST00000409689.5:c.1033+109_1033+115del	ENSP00000386263.1:n.1033+109_1033+115del
ENST00000469576.1:n.64+109_64+115del
ENST00000521082.5:c.*1185+109_*1185+115del	ENSP00000430351.1:n.*1185+109_*1185+115del
NM_001031710.2:c.1177+109_1177+115del	NP_001026880.2:n.1177+109_1177+115del
NM_018846.4:c.1033+109_1033+115del	NP_061334.4:n.1033+109_1033+115del
NR_033328.1:n.1601+109_1601+115del
XM_006715753.1:c.1216+109_1216+115del	XP_006715816.1:n.1216+109_1216+115del
XM_006715754.1:c.1150+109_1150+115del	XP_006715817.1:n.1150+109_1150+115del
XM_006715755.1:c.1150+109_1150+115del	XP_006715818.1:n.1150+109_1150+115del
XM_006715756.1:c.1072+109_1072+115del	XP_006715819.1:n.1072+109_1072+115del
XM_006715753.3:c.1216+109_1216+115del	XP_006715816.1:n.1216+109_1216+115del
XM_006715754.3:c.1150+109_1150+115del	XP_006715817.1:n.1150+109_1150+115del
XM_006715755.3:c.1150+109_1150+115del	XP_006715818.1:n.1150+109_1150+115del
XM_006715756.3:c.1072+109_1072+115del	XP_006715819.1:n.1072+109_1072+115del
XM_017012439.2:c.1111+109_1111+115del	XP_016867928.1:n.1111+109_1111+115del
NM_001031710.3:c.1177+109_1177+115del MANE Select	NP_001026880.2:n.1177+109_1177+115del
NM_018846.5:c.1033+109_1033+115del	NP_061334.4:n.1033+109_1033+115del
NR_033328.2:n.1550+109_1550+115del