Canonical Allele Identifier: CA2201646852

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447422G= , CM000678.2:g.1447422G=	GRCh38
NC_000016.9:g.1497423G= , CM000678.1:g.1497423G=	GRCh37
NC_000016.8:g.1437424G=	NCBI36
NG_007567.1:g.32663C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2220C=	ENSP00000514703.1:p.Phe740=
ENST00000699948.1:c.*533C=	ENSP00000514704.1:n.*533C=
ENST00000382745.9:c.2220C= MANE Select	ENSP00000372193.4:p.Phe740=
ENST00000262318.12:c.2148C=	ENSP00000262318.8:p.Phe716=
ENST00000382745.8:c.2220C=	ENSP00000372193.4:p.Phe740=
ENST00000448525.5:c.2148C=	ENSP00000410907.1:p.Phe716=
ENST00000563642.6:n.2289C=
ENST00000565092.6:n.1255C=
ENST00000567836.2:n.461C=
NM_001114331.2:c.2148C=	NP_001107803.1:p.Phe716=
NM_001287.5:c.2220C=	NP_001278.1:p.Phe740=
XM_011522354.1:c.2046C=	XP_011520656.1:p.Phe682=
NM_001287.6:c.2220C= MANE Select	NP_001278.1:p.Phe740=
NM_001114331.3:c.2148C=	NP_001107803.1:p.Phe716=