Canonical Allele Identifier: CA2774715124

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166029_23166030insA , CM000669.2:g.23166029_23166030insA	GRCh38
NC_000007.13:g.23205648_23205649insA , CM000669.1:g.23205648_23205649insA	GRCh37
NC_000007.12:g.23172173_23172174insA	NCBI36
NG_016983.1:g.65296_65297insA
NG_016983.2:g.65296_65297insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+91_1177+92insA MANE Select	ENSP00000343273.4:n.1177+91_1177+92insA
ENST00000339077.9:c.1177+91_1177+92insA	ENSP00000343273.4:n.1177+91_1177+92insA
ENST00000409689.5:c.1033+91_1033+92insA	ENSP00000386263.1:n.1033+91_1033+92insA
ENST00000469576.1:n.64+91_64+92insA
ENST00000521082.5:c.*1185+91_*1185+92insA	ENSP00000430351.1:n.*1185+91_*1185+92insA
NM_001031710.2:c.1177+91_1177+92insA	NP_001026880.2:n.1177+91_1177+92insA
NM_018846.4:c.1033+91_1033+92insA	NP_061334.4:n.1033+91_1033+92insA
NR_033328.1:n.1601+91_1601+92insA
XM_006715753.1:c.1216+91_1216+92insA	XP_006715816.1:n.1216+91_1216+92insA
XM_006715754.1:c.1150+91_1150+92insA	XP_006715817.1:n.1150+91_1150+92insA
XM_006715755.1:c.1150+91_1150+92insA	XP_006715818.1:n.1150+91_1150+92insA
XM_006715756.1:c.1072+91_1072+92insA	XP_006715819.1:n.1072+91_1072+92insA
XM_006715753.3:c.1216+91_1216+92insA	XP_006715816.1:n.1216+91_1216+92insA
XM_006715754.3:c.1150+91_1150+92insA	XP_006715817.1:n.1150+91_1150+92insA
XM_006715755.3:c.1150+91_1150+92insA	XP_006715818.1:n.1150+91_1150+92insA
XM_006715756.3:c.1072+91_1072+92insA	XP_006715819.1:n.1072+91_1072+92insA
XM_017012439.2:c.1111+91_1111+92insA	XP_016867928.1:n.1111+91_1111+92insA
NM_001031710.3:c.1177+91_1177+92insA MANE Select	NP_001026880.2:n.1177+91_1177+92insA
NM_018846.5:c.1033+91_1033+92insA	NP_061334.4:n.1033+91_1033+92insA
NR_033328.2:n.1550+91_1550+92insA