Canonical Allele Identifier: CA2774715157

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166065_23166066insA , CM000669.2:g.23166065_23166066insA	GRCh38
NC_000007.13:g.23205684_23205685insA , CM000669.1:g.23205684_23205685insA	GRCh37
NC_000007.12:g.23172209_23172210insA	NCBI36
NG_016983.1:g.65332_65333insA
NG_016983.2:g.65332_65333insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+127_1177+128insA MANE Select	ENSP00000343273.4:n.1177+127_1177+128insA
ENST00000339077.9:c.1177+127_1177+128insA	ENSP00000343273.4:n.1177+127_1177+128insA
ENST00000409689.5:c.1033+127_1033+128insA	ENSP00000386263.1:n.1033+127_1033+128insA
ENST00000469576.1:n.64+127_64+128insA
ENST00000521082.5:c.*1185+127_*1185+128insA	ENSP00000430351.1:n.*1185+127_*1185+128insA
NM_001031710.2:c.1177+127_1177+128insA	NP_001026880.2:n.1177+127_1177+128insA
NM_018846.4:c.1033+127_1033+128insA	NP_061334.4:n.1033+127_1033+128insA
NR_033328.1:n.1601+127_1601+128insA
XM_006715753.1:c.1216+127_1216+128insA	XP_006715816.1:n.1216+127_1216+128insA
XM_006715754.1:c.1150+127_1150+128insA	XP_006715817.1:n.1150+127_1150+128insA
XM_006715755.1:c.1150+127_1150+128insA	XP_006715818.1:n.1150+127_1150+128insA
XM_006715756.1:c.1072+127_1072+128insA	XP_006715819.1:n.1072+127_1072+128insA
XM_006715753.3:c.1216+127_1216+128insA	XP_006715816.1:n.1216+127_1216+128insA
XM_006715754.3:c.1150+127_1150+128insA	XP_006715817.1:n.1150+127_1150+128insA
XM_006715755.3:c.1150+127_1150+128insA	XP_006715818.1:n.1150+127_1150+128insA
XM_006715756.3:c.1072+127_1072+128insA	XP_006715819.1:n.1072+127_1072+128insA
XM_017012439.2:c.1111+127_1111+128insA	XP_016867928.1:n.1111+127_1111+128insA
NM_001031710.3:c.1177+127_1177+128insA MANE Select	NP_001026880.2:n.1177+127_1177+128insA
NM_018846.5:c.1033+127_1033+128insA	NP_061334.4:n.1033+127_1033+128insA
NR_033328.2:n.1550+127_1550+128insA