Canonical Allele Identifier: CA2201646888

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447501G= , CM000678.2:g.1447501G=	GRCh38
NC_000016.9:g.1497502G= , CM000678.1:g.1497502G=	GRCh37
NC_000016.8:g.1437503G=	NCBI36
NG_007567.1:g.32584C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699947.1:c.2141C=	ENSP00000514703.1:p.Ala714=
ENST00000699948.1:c.*454C=	ENSP00000514704.1:n.*454C=
ENST00000382745.9:c.2141C= MANE Select	ENSP00000372193.4:p.Ala714=
ENST00000262318.12:c.2069C=	ENSP00000262318.8:p.Ala690=
ENST00000382745.8:c.2141C=	ENSP00000372193.4:p.Ala714=
ENST00000448525.5:c.2069C=	ENSP00000410907.1:p.Ala690=
ENST00000563642.6:n.2210C=
ENST00000565092.6:n.1176C=
ENST00000567836.2:n.382C=
NM_001114331.2:c.2069C=	NP_001107803.1:p.Ala690=
NM_001287.5:c.2141C=	NP_001278.1:p.Ala714=
XM_011522354.1:c.1967C=	XP_011520656.1:p.Ala656=
NM_001287.6:c.2141C= MANE Select	NP_001278.1:p.Ala714=
NM_001114331.3:c.2069C=	NP_001107803.1:p.Ala690=