Canonical Allele Identifier: CA1694330789

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165821T= , CM000669.2:g.23165821T=	GRCh38
NC_000007.13:g.23205440T= , CM000669.1:g.23205440T=	GRCh37
NC_000007.12:g.23171965T=	NCBI36
NG_016983.1:g.65088T=
NG_016983.2:g.65088T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1060T= MANE Select	ENSP00000343273.4:p.Cys354=
ENST00000339077.9:c.1060T=	ENSP00000343273.4:p.Cys354=
ENST00000409689.5:c.916T=	ENSP00000386263.1:p.Cys306=
ENST00000521082.5:c.*1068T=	ENSP00000430351.1:n.*1068T=
NM_001031710.2:c.1060T=	NP_001026880.2:p.Cys354=
NM_018846.4:c.916T=	NP_061334.4:p.Cys306=
NR_033328.1:n.1484T=
XM_006715753.1:c.1099T=	XP_006715816.1:p.Cys367=
XM_006715754.1:c.1033T=	XP_006715817.1:p.Cys345=
XM_006715755.1:c.1033T=	XP_006715818.1:p.Cys345=
XM_006715756.1:c.955T=	XP_006715819.1:p.Cys319=
XM_006715753.3:c.1099T=	XP_006715816.1:p.Cys367=
XM_006715754.3:c.1033T=	XP_006715817.1:p.Cys345=
XM_006715755.3:c.1033T=	XP_006715818.1:p.Cys345=
XM_006715756.3:c.955T=	XP_006715819.1:p.Cys319=
XM_017012439.2:c.994T=	XP_016867928.1:p.Cys332=
NM_001031710.3:c.1060T= MANE Select	NP_001026880.2:p.Cys354=
NM_018846.5:c.916T=	NP_061334.4:p.Cys306=
NR_033328.2:n.1433T=