Canonical Allele Identifier: CA1694330770

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165731_23165732delinsGA , CM000669.2:g.23165731_23165732delinsGA	GRCh38
NC_000007.13:g.23205350_23205351delinsGA , CM000669.1:g.23205350_23205351delinsGA	GRCh37
NC_000007.12:g.23171875_23171876delinsGA	NCBI36
NG_016983.1:g.64998_64999delinsGA
NG_016983.2:g.64998_64999delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.970_971delinsGA MANE Select	ENSP00000343273.4:p.Glu324=
ENST00000339077.9:c.970_971delinsGA	ENSP00000343273.4:p.Glu324=
ENST00000409689.5:c.826_827delinsGA	ENSP00000386263.1:p.Glu276=
ENST00000521082.5:c.*978_*979delinsGA	ENSP00000430351.1:n.*978_*979delinsGA
NM_001031710.2:c.970_971delinsGA	NP_001026880.2:p.Glu324=
NM_018846.4:c.826_827delinsGA	NP_061334.4:p.Glu276=
NR_033328.1:n.1394_1395delinsGA
XM_006715753.1:c.1009_1010delinsGA	XP_006715816.1:p.Glu337=
XM_006715754.1:c.943_944delinsGA	XP_006715817.1:p.Glu315=
XM_006715755.1:c.943_944delinsGA	XP_006715818.1:p.Glu315=
XM_006715756.1:c.865_866delinsGA	XP_006715819.1:p.Glu289=
XM_006715753.3:c.1009_1010delinsGA	XP_006715816.1:p.Glu337=
XM_006715754.3:c.943_944delinsGA	XP_006715817.1:p.Glu315=
XM_006715755.3:c.943_944delinsGA	XP_006715818.1:p.Glu315=
XM_006715756.3:c.865_866delinsGA	XP_006715819.1:p.Glu289=
XM_017012439.2:c.904_905delinsGA	XP_016867928.1:p.Glu302=
NM_001031710.3:c.970_971delinsGA MANE Select	NP_001026880.2:p.Glu324=
NM_018846.5:c.826_827delinsGA	NP_061334.4:p.Glu276=
NR_033328.2:n.1343_1344delinsGA