Canonical Allele Identifier: CA1694330784

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165782T= , CM000669.2:g.23165782T=	GRCh38
NC_000007.13:g.23205401T= , CM000669.1:g.23205401T=	GRCh37
NC_000007.12:g.23171926T=	NCBI36
NG_016983.1:g.65049T=
NG_016983.2:g.65049T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1021T= MANE Select	ENSP00000343273.4:p.Leu341=
ENST00000339077.9:c.1021T=	ENSP00000343273.4:p.Leu341=
ENST00000409689.5:c.877T=	ENSP00000386263.1:p.Leu293=
ENST00000521082.5:c.*1029T=	ENSP00000430351.1:n.*1029T=
NM_001031710.2:c.1021T=	NP_001026880.2:p.Leu341=
NM_018846.4:c.877T=	NP_061334.4:p.Leu293=
NR_033328.1:n.1445T=
XM_006715753.1:c.1060T=	XP_006715816.1:p.Leu354=
XM_006715754.1:c.994T=	XP_006715817.1:p.Leu332=
XM_006715755.1:c.994T=	XP_006715818.1:p.Leu332=
XM_006715756.1:c.916T=	XP_006715819.1:p.Leu306=
XM_006715753.3:c.1060T=	XP_006715816.1:p.Leu354=
XM_006715754.3:c.994T=	XP_006715817.1:p.Leu332=
XM_006715755.3:c.994T=	XP_006715818.1:p.Leu332=
XM_006715756.3:c.916T=	XP_006715819.1:p.Leu306=
XM_017012439.2:c.955T=	XP_016867928.1:p.Leu319=
NM_001031710.3:c.1021T= MANE Select	NP_001026880.2:p.Leu341=
NM_018846.5:c.877T=	NP_061334.4:p.Leu293=
NR_033328.2:n.1394T=