Canonical Allele Identifier: CA7809906

Gene: CLCN7

Linked Data

• ClinVar Variation Id: 1429924
• ClinVar RCV Id: RCV001939172 ; RCV002560654
• dbSNP Id: rs767382071
• ExAC: 16:1497503 C / T
• gnomAD v2: 16-1497503-C-T
• gnomAD v3: 16-1447502-C-T
• gnomAD v4: 16-1447502-C-T
• MyVariant Identifiers: chr16:g.1497503C>T (hg19) ; chr16:g.1447502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447502C>T , CM000678.2:g.1447502C>T	GRCh38
NC_000016.9:g.1497503C>T , CM000678.1:g.1497503C>T	GRCh37
NC_000016.8:g.1437504C>T	NCBI36
NG_007567.1:g.32583G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699947.1:c.2140G>A	ENSP00000514703.1:p.Ala714Thr
ENST00000699948.1:c.*453G>A	ENSP00000514704.1:n.*453G>A
ENST00000382745.9:c.2140G>A MANE Select	ENSP00000372193.4:p.Ala714Thr
ENST00000262318.12:c.2068G>A	ENSP00000262318.8:p.Ala690Thr
ENST00000382745.8:c.2140G>A	ENSP00000372193.4:p.Ala714Thr
ENST00000448525.5:c.2068G>A	ENSP00000410907.1:p.Ala690Thr
ENST00000563642.6:n.2209G>A
ENST00000565092.6:n.1175G>A
ENST00000567836.2:n.381G>A
NM_001114331.2:c.2068G>A	NP_001107803.1:p.Ala690Thr
NM_001287.5:c.2140G>A	NP_001278.1:p.Ala714Thr
XM_011522354.1:c.1966G>A	XP_011520656.1:p.Ala656Thr
NM_001287.6:c.2140G>A MANE Select	NP_001278.1:p.Ala714Thr
NM_001114331.3:c.2068G>A	NP_001107803.1:p.Ala690Thr