Canonical Allele Identifier: CA492924273

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1460862-G-T
• MyVariant Identifiers: chr16:g.1510863G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1460862G>T , CM000678.2:g.1460862G>T	GRCh38
NC_000016.9:g.1510863G>T , CM000678.1:g.1510863G>T	GRCh37
NC_000016.8:g.1450864G>T	NCBI36
NG_007567.1:g.19223C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.438C>A	ENSP00000514703.1:p.Ile146=
ENST00000699948.1:c.438C>A	ENSP00000514704.1:p.Ile146=
ENST00000699950.1:n.390C>A
ENST00000382745.9:c.438C>A MANE Select	ENSP00000372193.4:p.Ile146=
ENST00000262318.12:c.366C>A	ENSP00000262318.8:p.Ile122=
ENST00000382745.8:c.438C>A	ENSP00000372193.4:p.Ile146=
ENST00000448525.5:c.366C>A	ENSP00000410907.1:p.Ile122=
ENST00000561665.5:n.468C>A
ENST00000564568.1:c.333C>A	ENSP00000454845.1:p.Ile111=
ENST00000567139.1:n.489C>A
ENST00000569851.6:c.264C>A	ENSP00000461009.1:p.Ile88=
NM_001114331.2:c.366C>A	NP_001107803.1:p.Ile122=
NM_001287.5:c.438C>A	NP_001278.1:p.Ile146=
XM_011522354.1:c.264C>A	XP_011520656.1:p.Ile88=
NM_001287.6:c.438C>A MANE Select	NP_001278.1:p.Ile146=
NM_001114331.3:c.366C>A	NP_001107803.1:p.Ile122=