Canonical Allele Identifier: CA1139768544

Gene: CLCN7

Linked Data

• dbSNP Id: rs777172728

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447000G>C , CM000678.2:g.1447000G>C	GRCh38
NC_000016.9:g.1497001G>C , CM000678.1:g.1497001G>C	GRCh37
NC_000016.8:g.1437002G>C	NCBI36
NG_007567.1:g.33085C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2331+6C>G	ENSP00000514703.1:n.2331+6C>G
ENST00000699948.1:c.*644+6C>G	ENSP00000514704.1:n.*644+6C>G
ENST00000382745.9:c.2331+6C>G MANE Select	ENSP00000372193.4:n.2331+6C>G
ENST00000262318.12:c.2260+6C>G	ENSP00000262318.8:n.2260+6C>G
ENST00000382745.8:c.2331+6C>G	ENSP00000372193.4:n.2331+6C>G
ENST00000448525.5:c.2259+6C>G	ENSP00000410907.1:n.2259+6C>G
ENST00000563642.6:n.2400+6C>G
ENST00000565092.6:n.1366+6C>G
ENST00000567836.2:n.572+6C>G
NM_001114331.2:c.2259+6C>G	NP_001107803.1:n.2259+6C>G
NM_001287.5:c.2331+6C>G	NP_001278.1:n.2331+6C>G
XM_011522354.1:c.2157+6C>G	XP_011520656.1:n.2157+6C>G
NM_001287.6:c.2331+6C>G MANE Select	NP_001278.1:n.2331+6C>G
NM_001114331.3:c.2259+6C>G	NP_001107803.1:n.2259+6C>G