Canonical Allele Identifier: CA394185804

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1447558-T-G
• MyVariant Identifiers: chr16:g.1497559T>G (hg19) ; chr16:g.1447558T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447558T>G , CM000678.2:g.1447558T>G	GRCh38
NC_000016.9:g.1497559T>G , CM000678.1:g.1497559T>G	GRCh37
NC_000016.8:g.1437560T>G	NCBI36
NG_007567.1:g.32527A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2084A>C	ENSP00000514703.1:p.Glu695Ala
ENST00000699948.1:c.*397A>C	ENSP00000514704.1:n.*397A>C
ENST00000382745.9:c.2084A>C MANE Select	ENSP00000372193.4:p.Glu695Ala
ENST00000262318.12:c.2012A>C	ENSP00000262318.8:p.Glu671Ala
ENST00000382745.8:c.2084A>C	ENSP00000372193.4:p.Glu695Ala
ENST00000448525.5:c.2012A>C	ENSP00000410907.1:p.Glu671Ala
ENST00000563642.6:n.2153A>C
ENST00000565092.6:n.1119A>C
ENST00000567836.2:n.325A>C
NM_001114331.2:c.2012A>C	NP_001107803.1:p.Glu671Ala
NM_001287.5:c.2084A>C	NP_001278.1:p.Glu695Ala
XM_011522354.1:c.1910A>C	XP_011520656.1:p.Glu637Ala
NM_001287.6:c.2084A>C MANE Select	NP_001278.1:p.Glu695Ala
NM_001114331.3:c.2012A>C	NP_001107803.1:p.Glu671Ala