Canonical Allele Identifier: CA2630991065

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1447579-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447582_1447583del , CM000678.2:g.1447582_1447583del	GRCh38
NC_000016.9:g.1497583_1497584del , CM000678.1:g.1497583_1497584del	GRCh37
NC_000016.8:g.1437584_1437585del	NCBI36
NG_007567.1:g.32504_32505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2074-13_2074-12del	ENSP00000514703.1:n.2074-13_2074-12del
ENST00000699948.1:c.*387-13_*387-12del	ENSP00000514704.1:n.*387-13_*387-12del
ENST00000382745.9:c.2074-13_2074-12del MANE Select	ENSP00000372193.4:n.2074-13_2074-12del
ENST00000262318.12:c.2002-13_2002-12del	ENSP00000262318.8:n.2002-13_2002-12del
ENST00000382745.8:c.2074-13_2074-12del	ENSP00000372193.4:n.2074-13_2074-12del
ENST00000448525.5:c.2002-13_2002-12del	ENSP00000410907.1:n.2002-13_2002-12del
ENST00000563642.6:n.2143-13_2143-12del
ENST00000565092.6:n.1109-13_1109-12del
ENST00000567836.2:n.315-13_315-12del
NM_001114331.2:c.2002-13_2002-12del	NP_001107803.1:n.2002-13_2002-12del
NM_001287.5:c.2074-13_2074-12del	NP_001278.1:n.2074-13_2074-12del
XM_011522354.1:c.1900-13_1900-12del	XP_011520656.1:n.1900-13_1900-12del
NM_001287.6:c.2074-13_2074-12del MANE Select	NP_001278.1:n.2074-13_2074-12del
NM_001114331.3:c.2002-13_2002-12del	NP_001107803.1:n.2002-13_2002-12del