Canonical Allele Identifier: CA2201679171

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1460959_1460970delinsCGGTCAGGGCGA , CM000678.2:g.1460959_1460970delinsCGGTCAGGGCGA	GRCh38
NC_000016.9:g.1510960_1510971delinsCGGTCAGGGCGA , CM000678.1:g.1510960_1510971delinsCGGTCAGGGCGA	GRCh37
NC_000016.8:g.1450961_1450972delinsCGGTCAGGGCGA	NCBI36
NG_007567.1:g.19115_19126delinsTCGCCCTGACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.352-22_352-11delinsTCGCCCTGACCG	ENSP00000514703.1:n.352-22_352-11delinsTCGCCCTGACCG
ENST00000699948.1:c.352-22_352-11delinsTCGCCCTGACCG	ENSP00000514704.1:n.352-22_352-11delinsTCGCCCTGACCG
ENST00000699950.1:n.304-22_304-11delinsTCGCCCTGACCG
ENST00000382745.9:c.352-22_352-11delinsTCGCCCTGACCG MANE Select	ENSP00000372193.4:n.352-22_352-11delinsTCGCCCTGACCG
ENST00000262318.12:c.280-22_280-11delinsTCGCCCTGACCG	ENSP00000262318.8:n.280-22_280-11delinsTCGCCCTGACCG
ENST00000382745.8:c.352-22_352-11delinsTCGCCCTGACCG	ENSP00000372193.4:n.352-22_352-11delinsTCGCCCTGACCG
ENST00000448525.5:c.280-22_280-11delinsTCGCCCTGACCG	ENSP00000410907.1:n.280-22_280-11delinsTCGCCCTGACCG
ENST00000561665.5:n.382-22_382-11delinsTCGCCCTGACCG
ENST00000564568.1:c.247-22_247-11delinsTCGCCCTGACCG	ENSP00000454845.1:n.247-22_247-11delinsTCGCCCTGACCG
ENST00000567139.1:n.403-22_403-11delinsTCGCCCTGACCG
ENST00000569851.6:c.178-22_178-11delinsTCGCCCTGACCG	ENSP00000461009.1:n.178-22_178-11delinsTCGCCCTGACCG
NM_001114331.2:c.280-22_280-11delinsTCGCCCTGACCG	NP_001107803.1:n.280-22_280-11delinsTCGCCCTGACCG
NM_001287.5:c.352-22_352-11delinsTCGCCCTGACCG	NP_001278.1:n.352-22_352-11delinsTCGCCCTGACCG
XM_011522354.1:c.178-22_178-11delinsTCGCCCTGACCG	XP_011520656.1:n.178-22_178-11delinsTCGCCCTGACCG
NM_001287.6:c.352-22_352-11delinsTCGCCCTGACCG MANE Select	NP_001278.1:n.352-22_352-11delinsTCGCCCTGACCG
NM_001114331.3:c.280-22_280-11delinsTCGCCCTGACCG	NP_001107803.1:n.280-22_280-11delinsTCGCCCTGACCG