Canonical Allele Identifier: CA2774715164

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166072_23166073insA , CM000669.2:g.23166072_23166073insA	GRCh38
NC_000007.13:g.23205691_23205692insA , CM000669.1:g.23205691_23205692insA	GRCh37
NC_000007.12:g.23172216_23172217insA	NCBI36
NG_016983.1:g.65339_65340insA
NG_016983.2:g.65339_65340insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+134_1177+135insA MANE Select	ENSP00000343273.4:n.1177+134_1177+135insA
ENST00000339077.9:c.1177+134_1177+135insA	ENSP00000343273.4:n.1177+134_1177+135insA
ENST00000409689.5:c.1033+134_1033+135insA	ENSP00000386263.1:n.1033+134_1033+135insA
ENST00000469576.1:n.64+134_64+135insA
ENST00000521082.5:c.*1185+134_*1185+135insA	ENSP00000430351.1:n.*1185+134_*1185+135insA
NM_001031710.2:c.1177+134_1177+135insA	NP_001026880.2:n.1177+134_1177+135insA
NM_018846.4:c.1033+134_1033+135insA	NP_061334.4:n.1033+134_1033+135insA
NR_033328.1:n.1601+134_1601+135insA
XM_006715753.1:c.1216+134_1216+135insA	XP_006715816.1:n.1216+134_1216+135insA
XM_006715754.1:c.1150+134_1150+135insA	XP_006715817.1:n.1150+134_1150+135insA
XM_006715755.1:c.1150+134_1150+135insA	XP_006715818.1:n.1150+134_1150+135insA
XM_006715756.1:c.1072+134_1072+135insA	XP_006715819.1:n.1072+134_1072+135insA
XM_006715753.3:c.1216+134_1216+135insA	XP_006715816.1:n.1216+134_1216+135insA
XM_006715754.3:c.1150+134_1150+135insA	XP_006715817.1:n.1150+134_1150+135insA
XM_006715755.3:c.1150+134_1150+135insA	XP_006715818.1:n.1150+134_1150+135insA
XM_006715756.3:c.1072+134_1072+135insA	XP_006715819.1:n.1072+134_1072+135insA
XM_017012439.2:c.1111+134_1111+135insA	XP_016867928.1:n.1111+134_1111+135insA
NM_001031710.3:c.1177+134_1177+135insA MANE Select	NP_001026880.2:n.1177+134_1177+135insA
NM_018846.5:c.1033+134_1033+135insA	NP_061334.4:n.1033+134_1033+135insA
NR_033328.2:n.1550+134_1550+135insA