Canonical Allele Identifier: CA492916626

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1447485-T-G
• MyVariant Identifiers: chr16:g.1497486T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447485T>G , CM000678.2:g.1447485T>G	GRCh38
NC_000016.9:g.1497486T>G , CM000678.1:g.1497486T>G	GRCh37
NC_000016.8:g.1437487T>G	NCBI36
NG_007567.1:g.32600A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2157A>C	ENSP00000514703.1:p.Pro719=
ENST00000699948.1:c.*470A>C	ENSP00000514704.1:n.*470A>C
ENST00000382745.9:c.2157A>C MANE Select	ENSP00000372193.4:p.Pro719=
ENST00000262318.12:c.2085A>C	ENSP00000262318.8:p.Pro695=
ENST00000382745.8:c.2157A>C	ENSP00000372193.4:p.Pro719=
ENST00000448525.5:c.2085A>C	ENSP00000410907.1:p.Pro695=
ENST00000563642.6:n.2226A>C
ENST00000565092.6:n.1192A>C
ENST00000567836.2:n.398A>C
NM_001114331.2:c.2085A>C	NP_001107803.1:p.Pro695=
NM_001287.5:c.2157A>C	NP_001278.1:p.Pro719=
XM_011522354.1:c.1983A>C	XP_011520656.1:p.Pro661=
NM_001287.6:c.2157A>C MANE Select	NP_001278.1:p.Pro719=
NM_001114331.3:c.2085A>C	NP_001107803.1:p.Pro695=