Canonical Allele Identifier: CA394192501

Gene: CLCN7

Linked Data

• MyVariant Identifiers: chr16:g.1510869A>C (hg19) ; chr16:g.1460868A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1460868A>C , CM000678.2:g.1460868A>C	GRCh38
NC_000016.9:g.1510869A>C , CM000678.1:g.1510869A>C	GRCh37
NC_000016.8:g.1450870A>C	NCBI36
NG_007567.1:g.19217T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.432T>G	ENSP00000514703.1:p.Ile144Met
ENST00000699948.1:c.432T>G	ENSP00000514704.1:p.Ile144Met
ENST00000699950.1:n.384T>G
ENST00000382745.9:c.432T>G MANE Select	ENSP00000372193.4:p.Ile144Met
ENST00000262318.12:c.360T>G	ENSP00000262318.8:p.Ile120Met
ENST00000382745.8:c.432T>G	ENSP00000372193.4:p.Ile144Met
ENST00000448525.5:c.360T>G	ENSP00000410907.1:p.Ile120Met
ENST00000561665.5:n.462T>G
ENST00000564568.1:c.327T>G	ENSP00000454845.1:p.Ile109Met
ENST00000567139.1:n.483T>G
ENST00000569851.6:c.258T>G	ENSP00000461009.1:p.Ile86Met
NM_001114331.2:c.360T>G	NP_001107803.1:p.Ile120Met
NM_001287.5:c.432T>G	NP_001278.1:p.Ile144Met
XM_011522354.1:c.258T>G	XP_011520656.1:p.Ile86Met
NM_001287.6:c.432T>G MANE Select	NP_001278.1:p.Ile144Met
NM_001114331.3:c.360T>G	NP_001107803.1:p.Ile120Met