Canonical Allele Identifier: CA1694330785

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165790C= , CM000669.2:g.23165790C=	GRCh38
NC_000007.13:g.23205409C= , CM000669.1:g.23205409C=	GRCh37
NC_000007.12:g.23171934C=	NCBI36
NG_016983.1:g.65057C=
NG_016983.2:g.65057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1029C= MANE Select	ENSP00000343273.4:p.Gly343=
ENST00000339077.9:c.1029C=	ENSP00000343273.4:p.Gly343=
ENST00000409689.5:c.885C=	ENSP00000386263.1:p.Gly295=
ENST00000521082.5:c.*1037C=	ENSP00000430351.1:n.*1037C=
NM_001031710.2:c.1029C=	NP_001026880.2:p.Gly343=
NM_018846.4:c.885C=	NP_061334.4:p.Gly295=
NR_033328.1:n.1453C=
XM_006715753.1:c.1068C=	XP_006715816.1:p.Gly356=
XM_006715754.1:c.1002C=	XP_006715817.1:p.Gly334=
XM_006715755.1:c.1002C=	XP_006715818.1:p.Gly334=
XM_006715756.1:c.924C=	XP_006715819.1:p.Gly308=
XM_006715753.3:c.1068C=	XP_006715816.1:p.Gly356=
XM_006715754.3:c.1002C=	XP_006715817.1:p.Gly334=
XM_006715755.3:c.1002C=	XP_006715818.1:p.Gly334=
XM_006715756.3:c.924C=	XP_006715819.1:p.Gly308=
XM_017012439.2:c.963C=	XP_016867928.1:p.Gly321=
NM_001031710.3:c.1029C= MANE Select	NP_001026880.2:p.Gly343=
NM_018846.5:c.885C=	NP_061334.4:p.Gly295=
NR_033328.2:n.1402C=