Canonical Allele Identifier: CA276668092

Gene: CLCN7

Linked Data

• ClinVar Variation Id: 1498507
• ClinVar RCV Id: RCV002035568
• dbSNP Id: rs1032308852
• gnomAD v2: 16-1497556-C-A
• gnomAD v3: 16-1447555-C-A
• gnomAD v4: 16-1447555-C-A
• MyVariant Identifiers: chr16:g.1497556C>A (hg19) ; chr16:g.1447555C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447555C>A , CM000678.2:g.1447555C>A	GRCh38
NC_000016.9:g.1497556C>A , CM000678.1:g.1497556C>A	GRCh37
NC_000016.8:g.1437557C>A	NCBI36
NG_007567.1:g.32530G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2087G>T	ENSP00000514703.1:p.Arg696Leu
ENST00000699948.1:c.*400G>T	ENSP00000514704.1:n.*400G>T
ENST00000382745.9:c.2087G>T MANE Select	ENSP00000372193.4:p.Arg696Leu
ENST00000262318.12:c.2015G>T	ENSP00000262318.8:p.Arg672Leu
ENST00000382745.8:c.2087G>T	ENSP00000372193.4:p.Arg696Leu
ENST00000448525.5:c.2015G>T	ENSP00000410907.1:p.Arg672Leu
ENST00000563642.6:n.2156G>T
ENST00000565092.6:n.1122G>T
ENST00000567836.2:n.328G>T
NM_001114331.2:c.2015G>T	NP_001107803.1:p.Arg672Leu
NM_001287.5:c.2087G>T	NP_001278.1:p.Arg696Leu
XM_011522354.1:c.1913G>T	XP_011520656.1:p.Arg638Leu
NM_001287.6:c.2087G>T MANE Select	NP_001278.1:p.Arg696Leu
NM_001114331.3:c.2015G>T	NP_001107803.1:p.Arg672Leu