Canonical Allele Identifier: CA1694330811

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165902G= , CM000669.2:g.23165902G=	GRCh38
NC_000007.13:g.23205521G= , CM000669.1:g.23205521G=	GRCh37
NC_000007.12:g.23172046G=	NCBI36
NG_016983.1:g.65169G=
NG_016983.2:g.65169G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1141G= MANE Select	ENSP00000343273.4:p.Glu381=
ENST00000339077.9:c.1141G=	ENSP00000343273.4:p.Glu381=
ENST00000409689.5:c.997G=	ENSP00000386263.1:p.Glu333=
ENST00000469576.1:n.28G=
ENST00000521082.5:c.*1149G=	ENSP00000430351.1:n.*1149G=
NM_001031710.2:c.1141G=	NP_001026880.2:p.Glu381=
NM_018846.4:c.997G=	NP_061334.4:p.Glu333=
NR_033328.1:n.1565G=
XM_006715753.1:c.1180G=	XP_006715816.1:p.Glu394=
XM_006715754.1:c.1114G=	XP_006715817.1:p.Glu372=
XM_006715755.1:c.1114G=	XP_006715818.1:p.Glu372=
XM_006715756.1:c.1036G=	XP_006715819.1:p.Glu346=
XM_006715753.3:c.1180G=	XP_006715816.1:p.Glu394=
XM_006715754.3:c.1114G=	XP_006715817.1:p.Glu372=
XM_006715755.3:c.1114G=	XP_006715818.1:p.Glu372=
XM_006715756.3:c.1036G=	XP_006715819.1:p.Glu346=
XM_017012439.2:c.1075G=	XP_016867928.1:p.Glu359=
NM_001031710.3:c.1141G= MANE Select	NP_001026880.2:p.Glu381=
NM_018846.5:c.997G=	NP_061334.4:p.Glu333=
NR_033328.2:n.1514G=