Canonical Allele Identifier: CA1694330775

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165751A= , CM000669.2:g.23165751A=	GRCh38
NC_000007.13:g.23205370A= , CM000669.1:g.23205370A=	GRCh37
NC_000007.12:g.23171895A=	NCBI36
NG_016983.1:g.65018A=
NG_016983.2:g.65018A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.990A= MANE Select	ENSP00000343273.4:p.Ala330=
ENST00000339077.9:c.990A=	ENSP00000343273.4:p.Ala330=
ENST00000409689.5:c.846A=	ENSP00000386263.1:p.Ala282=
ENST00000521082.5:c.*998A=	ENSP00000430351.1:n.*998A=
NM_001031710.2:c.990A=	NP_001026880.2:p.Ala330=
NM_018846.4:c.846A=	NP_061334.4:p.Ala282=
NR_033328.1:n.1414A=
XM_006715753.1:c.1029A=	XP_006715816.1:p.Ala343=
XM_006715754.1:c.963A=	XP_006715817.1:p.Ala321=
XM_006715755.1:c.963A=	XP_006715818.1:p.Ala321=
XM_006715756.1:c.885A=	XP_006715819.1:p.Ala295=
XM_006715753.3:c.1029A=	XP_006715816.1:p.Ala343=
XM_006715754.3:c.963A=	XP_006715817.1:p.Ala321=
XM_006715755.3:c.963A=	XP_006715818.1:p.Ala321=
XM_006715756.3:c.885A=	XP_006715819.1:p.Ala295=
XM_017012439.2:c.924A=	XP_016867928.1:p.Ala308=
NM_001031710.3:c.990A= MANE Select	NP_001026880.2:p.Ala330=
NM_018846.5:c.846A=	NP_061334.4:p.Ala282=
NR_033328.2:n.1363A=