Canonical Allele Identifier: CA2774715099

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166006_23166011del , CM000669.2:g.23166006_23166011del	GRCh38
NC_000007.13:g.23205625_23205630del , CM000669.1:g.23205625_23205630del	GRCh37
NC_000007.12:g.23172150_23172155del	NCBI36
NG_016983.1:g.65273_65278del
NG_016983.2:g.65273_65278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+68_1177+73del MANE Select	ENSP00000343273.4:n.1177+68_1177+73del
ENST00000339077.9:c.1177+68_1177+73del	ENSP00000343273.4:n.1177+68_1177+73del
ENST00000409689.5:c.1033+68_1033+73del	ENSP00000386263.1:n.1033+68_1033+73del
ENST00000469576.1:n.64+68_64+73del
ENST00000521082.5:c.*1185+68_*1185+73del	ENSP00000430351.1:n.*1185+68_*1185+73del
NM_001031710.2:c.1177+68_1177+73del	NP_001026880.2:n.1177+68_1177+73del
NM_018846.4:c.1033+68_1033+73del	NP_061334.4:n.1033+68_1033+73del
NR_033328.1:n.1601+68_1601+73del
XM_006715753.1:c.1216+68_1216+73del	XP_006715816.1:n.1216+68_1216+73del
XM_006715754.1:c.1150+68_1150+73del	XP_006715817.1:n.1150+68_1150+73del
XM_006715755.1:c.1150+68_1150+73del	XP_006715818.1:n.1150+68_1150+73del
XM_006715756.1:c.1072+68_1072+73del	XP_006715819.1:n.1072+68_1072+73del
XM_006715753.3:c.1216+68_1216+73del	XP_006715816.1:n.1216+68_1216+73del
XM_006715754.3:c.1150+68_1150+73del	XP_006715817.1:n.1150+68_1150+73del
XM_006715755.3:c.1150+68_1150+73del	XP_006715818.1:n.1150+68_1150+73del
XM_006715756.3:c.1072+68_1072+73del	XP_006715819.1:n.1072+68_1072+73del
XM_017012439.2:c.1111+68_1111+73del	XP_016867928.1:n.1111+68_1111+73del
NM_001031710.3:c.1177+68_1177+73del MANE Select	NP_001026880.2:n.1177+68_1177+73del
NM_018846.5:c.1033+68_1033+73del	NP_061334.4:n.1033+68_1033+73del
NR_033328.2:n.1550+68_1550+73del