Canonical Allele Identifier: CA2201646874

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447467G= , CM000678.2:g.1447467G=	GRCh38
NC_000016.9:g.1497468G= , CM000678.1:g.1497468G=	GRCh37
NC_000016.8:g.1437469G=	NCBI36
NG_007567.1:g.32618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2175C=	ENSP00000514703.1:p.His725=
ENST00000699948.1:c.*488C=	ENSP00000514704.1:n.*488C=
ENST00000382745.9:c.2175C= MANE Select	ENSP00000372193.4:p.His725=
ENST00000262318.12:c.2103C=	ENSP00000262318.8:p.His701=
ENST00000382745.8:c.2175C=	ENSP00000372193.4:p.His725=
ENST00000448525.5:c.2103C=	ENSP00000410907.1:p.His701=
ENST00000563642.6:n.2244C=
ENST00000565092.6:n.1210C=
ENST00000567836.2:n.416C=
NM_001114331.2:c.2103C=	NP_001107803.1:p.His701=
NM_001287.5:c.2175C=	NP_001278.1:p.His725=
XM_011522354.1:c.2001C=	XP_011520656.1:p.His667=
NM_001287.6:c.2175C= MANE Select	NP_001278.1:p.His725=
NM_001114331.3:c.2103C=	NP_001107803.1:p.His701=