Canonical Allele Identifier: CA2630996401

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1460970-A-AGGGTCAGGCAGGGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1460971_1460986dup , CM000678.2:g.1460971_1460986dup	GRCh38
NC_000016.9:g.1510972_1510987dup , CM000678.1:g.1510972_1510987dup	GRCh37
NC_000016.8:g.1450973_1450988dup	NCBI36
NG_007567.1:g.19099_19114dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.352-38_352-23dup	ENSP00000514703.1:n.352-38_352-23dup
ENST00000699948.1:c.352-38_352-23dup	ENSP00000514704.1:n.352-38_352-23dup
ENST00000699950.1:n.304-38_304-23dup
ENST00000382745.9:c.352-38_352-23dup MANE Select	ENSP00000372193.4:n.352-38_352-23dup
ENST00000262318.12:c.280-38_280-23dup	ENSP00000262318.8:n.280-38_280-23dup
ENST00000382745.8:c.352-38_352-23dup	ENSP00000372193.4:n.352-38_352-23dup
ENST00000448525.5:c.280-38_280-23dup	ENSP00000410907.1:n.280-38_280-23dup
ENST00000561665.5:n.382-38_382-23dup
ENST00000564568.1:c.247-38_247-23dup	ENSP00000454845.1:n.247-38_247-23dup
ENST00000567139.1:n.403-38_403-23dup
ENST00000569851.6:c.178-38_178-23dup	ENSP00000461009.1:n.178-38_178-23dup
NM_001114331.2:c.280-38_280-23dup	NP_001107803.1:n.280-38_280-23dup
NM_001287.5:c.352-38_352-23dup	NP_001278.1:n.352-38_352-23dup
XM_011522354.1:c.178-38_178-23dup	XP_011520656.1:n.178-38_178-23dup
NM_001287.6:c.352-38_352-23dup MANE Select	NP_001278.1:n.352-38_352-23dup
NM_001114331.3:c.280-38_280-23dup	NP_001107803.1:n.280-38_280-23dup