Canonical Allele Identifier: CA2774715116

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166020_23166021insA , CM000669.2:g.23166020_23166021insA	GRCh38
NC_000007.13:g.23205639_23205640insA , CM000669.1:g.23205639_23205640insA	GRCh37
NC_000007.12:g.23172164_23172165insA	NCBI36
NG_016983.1:g.65287_65288insA
NG_016983.2:g.65287_65288insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+82_1177+83insA MANE Select	ENSP00000343273.4:n.1177+82_1177+83insA
ENST00000339077.9:c.1177+82_1177+83insA	ENSP00000343273.4:n.1177+82_1177+83insA
ENST00000409689.5:c.1033+82_1033+83insA	ENSP00000386263.1:n.1033+82_1033+83insA
ENST00000469576.1:n.64+82_64+83insA
ENST00000521082.5:c.*1185+82_*1185+83insA	ENSP00000430351.1:n.*1185+82_*1185+83insA
NM_001031710.2:c.1177+82_1177+83insA	NP_001026880.2:n.1177+82_1177+83insA
NM_018846.4:c.1033+82_1033+83insA	NP_061334.4:n.1033+82_1033+83insA
NR_033328.1:n.1601+82_1601+83insA
XM_006715753.1:c.1216+82_1216+83insA	XP_006715816.1:n.1216+82_1216+83insA
XM_006715754.1:c.1150+82_1150+83insA	XP_006715817.1:n.1150+82_1150+83insA
XM_006715755.1:c.1150+82_1150+83insA	XP_006715818.1:n.1150+82_1150+83insA
XM_006715756.1:c.1072+82_1072+83insA	XP_006715819.1:n.1072+82_1072+83insA
XM_006715753.3:c.1216+82_1216+83insA	XP_006715816.1:n.1216+82_1216+83insA
XM_006715754.3:c.1150+82_1150+83insA	XP_006715817.1:n.1150+82_1150+83insA
XM_006715755.3:c.1150+82_1150+83insA	XP_006715818.1:n.1150+82_1150+83insA
XM_006715756.3:c.1072+82_1072+83insA	XP_006715819.1:n.1072+82_1072+83insA
XM_017012439.2:c.1111+82_1111+83insA	XP_016867928.1:n.1111+82_1111+83insA
NM_001031710.3:c.1177+82_1177+83insA MANE Select	NP_001026880.2:n.1177+82_1177+83insA
NM_018846.5:c.1033+82_1033+83insA	NP_061334.4:n.1033+82_1033+83insA
NR_033328.2:n.1550+82_1550+83insA