Canonical Allele Identifier: CA2201646892

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447507_1447508delinsCG , CM000678.2:g.1447507_1447508delinsCG	GRCh38
NC_000016.9:g.1497508_1497509delinsCG , CM000678.1:g.1497508_1497509delinsCG	GRCh37
NC_000016.8:g.1437509_1437510delinsCG	NCBI36
NG_007567.1:g.32577_32578delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000699947.1:c.2134_2135delinsCG	ENSP00000514703.1:p.Arg712=
ENST00000699948.1:c.*447_*448delinsCG	ENSP00000514704.1:n.*447_*448delinsCG
ENST00000382745.9:c.2134_2135delinsCG MANE Select	ENSP00000372193.4:p.Arg712=
ENST00000262318.12:c.2062_2063delinsCG	ENSP00000262318.8:p.Arg688=
ENST00000382745.8:c.2134_2135delinsCG	ENSP00000372193.4:p.Arg712=
ENST00000448525.5:c.2062_2063delinsCG	ENSP00000410907.1:p.Arg688=
ENST00000563642.6:n.2203_2204delinsCG
ENST00000565092.6:n.1169_1170delinsCG
ENST00000567836.2:n.375_376delinsCG
NM_001114331.2:c.2062_2063delinsCG	NP_001107803.1:p.Arg688=
NM_001287.5:c.2134_2135delinsCG	NP_001278.1:p.Arg712=
XM_011522354.1:c.1960_1961delinsCG	XP_011520656.1:p.Arg654=
NM_001287.6:c.2134_2135delinsCG MANE Select	NP_001278.1:p.Arg712=
NM_001114331.3:c.2062_2063delinsCG	NP_001107803.1:p.Arg688=