Canonical Allele Identifier: CA1694330772

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165738G= , CM000669.2:g.23165738G=	GRCh38
NC_000007.13:g.23205357G= , CM000669.1:g.23205357G=	GRCh37
NC_000007.12:g.23171882G=	NCBI36
NG_016983.1:g.65005G=
NG_016983.2:g.65005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.977G= MANE Select	ENSP00000343273.4:p.Arg326=
ENST00000339077.9:c.977G=	ENSP00000343273.4:p.Arg326=
ENST00000409689.5:c.833G=	ENSP00000386263.1:p.Arg278=
ENST00000521082.5:c.*985G=	ENSP00000430351.1:n.*985G=
NM_001031710.2:c.977G=	NP_001026880.2:p.Arg326=
NM_018846.4:c.833G=	NP_061334.4:p.Arg278=
NR_033328.1:n.1401G=
XM_006715753.1:c.1016G=	XP_006715816.1:p.Arg339=
XM_006715754.1:c.950G=	XP_006715817.1:p.Arg317=
XM_006715755.1:c.950G=	XP_006715818.1:p.Arg317=
XM_006715756.1:c.872G=	XP_006715819.1:p.Arg291=
XM_006715753.3:c.1016G=	XP_006715816.1:p.Arg339=
XM_006715754.3:c.950G=	XP_006715817.1:p.Arg317=
XM_006715755.3:c.950G=	XP_006715818.1:p.Arg317=
XM_006715756.3:c.872G=	XP_006715819.1:p.Arg291=
XM_017012439.2:c.911G=	XP_016867928.1:p.Arg304=
NM_001031710.3:c.977G= MANE Select	NP_001026880.2:p.Arg326=
NM_018846.5:c.833G=	NP_061334.4:p.Arg278=
NR_033328.2:n.1350G=