Canonical Allele Identifier: CA2201646887

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447498T= , CM000678.2:g.1447498T=	GRCh38
NC_000016.9:g.1497499T= , CM000678.1:g.1497499T=	GRCh37
NC_000016.8:g.1437500T=	NCBI36
NG_007567.1:g.32587A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699947.1:c.2144A=	ENSP00000514703.1:p.Tyr715=
ENST00000699948.1:c.*457A=	ENSP00000514704.1:n.*457A=
ENST00000382745.9:c.2144A= MANE Select	ENSP00000372193.4:p.Tyr715=
ENST00000262318.12:c.2072A=	ENSP00000262318.8:p.Tyr691=
ENST00000382745.8:c.2144A=	ENSP00000372193.4:p.Tyr715=
ENST00000448525.5:c.2072A=	ENSP00000410907.1:p.Tyr691=
ENST00000563642.6:n.2213A=
ENST00000565092.6:n.1179A=
ENST00000567836.2:n.385A=
NM_001114331.2:c.2072A=	NP_001107803.1:p.Tyr691=
NM_001287.5:c.2144A=	NP_001278.1:p.Tyr715=
XM_011522354.1:c.1970A=	XP_011520656.1:p.Tyr657=
NM_001287.6:c.2144A= MANE Select	NP_001278.1:p.Tyr715=
NM_001114331.3:c.2072A=	NP_001107803.1:p.Tyr691=