Canonical Allele Identifier: CA2774715129

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166032_23166033insACT , CM000669.2:g.23166032_23166033insACT	GRCh38
NC_000007.13:g.23205651_23205652insACT , CM000669.1:g.23205651_23205652insACT	GRCh37
NC_000007.12:g.23172176_23172177insACT	NCBI36
NG_016983.1:g.65299_65300insACT
NG_016983.2:g.65299_65300insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+94_1177+95insACT MANE Select	ENSP00000343273.4:n.1177+94_1177+95insACT
ENST00000339077.9:c.1177+94_1177+95insACT	ENSP00000343273.4:n.1177+94_1177+95insACT
ENST00000409689.5:c.1033+94_1033+95insACT	ENSP00000386263.1:n.1033+94_1033+95insACT
ENST00000469576.1:n.64+94_64+95insACT
ENST00000521082.5:c.*1185+94_*1185+95insACT	ENSP00000430351.1:n.*1185+94_*1185+95insACT
NM_001031710.2:c.1177+94_1177+95insACT	NP_001026880.2:n.1177+94_1177+95insACT
NM_018846.4:c.1033+94_1033+95insACT	NP_061334.4:n.1033+94_1033+95insACT
NR_033328.1:n.1601+94_1601+95insACT
XM_006715753.1:c.1216+94_1216+95insACT	XP_006715816.1:n.1216+94_1216+95insACT
XM_006715754.1:c.1150+94_1150+95insACT	XP_006715817.1:n.1150+94_1150+95insACT
XM_006715755.1:c.1150+94_1150+95insACT	XP_006715818.1:n.1150+94_1150+95insACT
XM_006715756.1:c.1072+94_1072+95insACT	XP_006715819.1:n.1072+94_1072+95insACT
XM_006715753.3:c.1216+94_1216+95insACT	XP_006715816.1:n.1216+94_1216+95insACT
XM_006715754.3:c.1150+94_1150+95insACT	XP_006715817.1:n.1150+94_1150+95insACT
XM_006715755.3:c.1150+94_1150+95insACT	XP_006715818.1:n.1150+94_1150+95insACT
XM_006715756.3:c.1072+94_1072+95insACT	XP_006715819.1:n.1072+94_1072+95insACT
XM_017012439.2:c.1111+94_1111+95insACT	XP_016867928.1:n.1111+94_1111+95insACT
NM_001031710.3:c.1177+94_1177+95insACT MANE Select	NP_001026880.2:n.1177+94_1177+95insACT
NM_018846.5:c.1033+94_1033+95insACT	NP_061334.4:n.1033+94_1033+95insACT
NR_033328.2:n.1550+94_1550+95insACT