Canonical Allele Identifier: CA1694330808

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165895T= , CM000669.2:g.23165895T=	GRCh38
NC_000007.13:g.23205514T= , CM000669.1:g.23205514T=	GRCh37
NC_000007.12:g.23172039T=	NCBI36
NG_016983.1:g.65162T=
NG_016983.2:g.65162T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1134T= MANE Select	ENSP00000343273.4:p.Cys378=
ENST00000339077.9:c.1134T=	ENSP00000343273.4:p.Cys378=
ENST00000409689.5:c.990T=	ENSP00000386263.1:p.Cys330=
ENST00000469576.1:n.21T=
ENST00000521082.5:c.*1142T=	ENSP00000430351.1:n.*1142T=
NM_001031710.2:c.1134T=	NP_001026880.2:p.Cys378=
NM_018846.4:c.990T=	NP_061334.4:p.Cys330=
NR_033328.1:n.1558T=
XM_006715753.1:c.1173T=	XP_006715816.1:p.Cys391=
XM_006715754.1:c.1107T=	XP_006715817.1:p.Cys369=
XM_006715755.1:c.1107T=	XP_006715818.1:p.Cys369=
XM_006715756.1:c.1029T=	XP_006715819.1:p.Cys343=
XM_006715753.3:c.1173T=	XP_006715816.1:p.Cys391=
XM_006715754.3:c.1107T=	XP_006715817.1:p.Cys369=
XM_006715755.3:c.1107T=	XP_006715818.1:p.Cys369=
XM_006715756.3:c.1029T=	XP_006715819.1:p.Cys343=
XM_017012439.2:c.1068T=	XP_016867928.1:p.Cys356=
NM_001031710.3:c.1134T= MANE Select	NP_001026880.2:p.Cys378=
NM_018846.5:c.990T=	NP_061334.4:p.Cys330=
NR_033328.2:n.1507T=