Canonical Allele Identifier: CA1694330769

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165720G= , CM000669.2:g.23165720G=	GRCh38
NC_000007.13:g.23205339G= , CM000669.1:g.23205339G=	GRCh37
NC_000007.12:g.23171864G=	NCBI36
NG_016983.1:g.64987G=
NG_016983.2:g.64987G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.959G= MANE Select	ENSP00000343273.4:p.Arg320=
ENST00000339077.9:c.959G=	ENSP00000343273.4:p.Arg320=
ENST00000409689.5:c.815G=	ENSP00000386263.1:p.Arg272=
ENST00000521082.5:c.*967G=	ENSP00000430351.1:n.*967G=
NM_001031710.2:c.959G=	NP_001026880.2:p.Arg320=
NM_018846.4:c.815G=	NP_061334.4:p.Arg272=
NR_033328.1:n.1383G=
XM_006715753.1:c.998G=	XP_006715816.1:p.Arg333=
XM_006715754.1:c.932G=	XP_006715817.1:p.Arg311=
XM_006715755.1:c.932G=	XP_006715818.1:p.Arg311=
XM_006715756.1:c.854G=	XP_006715819.1:p.Arg285=
XM_006715753.3:c.998G=	XP_006715816.1:p.Arg333=
XM_006715754.3:c.932G=	XP_006715817.1:p.Arg311=
XM_006715755.3:c.932G=	XP_006715818.1:p.Arg311=
XM_006715756.3:c.854G=	XP_006715819.1:p.Arg285=
XM_017012439.2:c.893G=	XP_016867928.1:p.Arg298=
NM_001031710.3:c.959G= MANE Select	NP_001026880.2:p.Arg320=
NM_018846.5:c.815G=	NP_061334.4:p.Arg272=
NR_033328.2:n.1332G=