Canonical Allele Identifier: CA492924282

Gene: CLCN7

Linked Data

• MyVariant Identifiers: chr16:g.1510869A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000699947.1:c.432T>C	ENSP00000514703.1:p.Ile144=
ENST00000699948.1:c.432T>C	ENSP00000514704.1:p.Ile144=
ENST00000699950.1:n.384T>C
ENST00000382745.9:c.432T>C MANE Select	ENSP00000372193.4:p.Ile144=
ENST00000262318.12:c.360T>C	ENSP00000262318.8:p.Ile120=
ENST00000382745.8:c.432T>C	ENSP00000372193.4:p.Ile144=
ENST00000448525.5:c.360T>C	ENSP00000410907.1:p.Ile120=
ENST00000561665.5:n.462T>C
ENST00000564568.1:c.327T>C	ENSP00000454845.1:p.Ile109=
ENST00000567139.1:n.483T>C
ENST00000569851.6:c.258T>C	ENSP00000461009.1:p.Ile86=
NM_001114331.2:c.360T>C	NP_001107803.1:p.Ile120=
NM_001287.5:c.432T>C	NP_001278.1:p.Ile144=
XM_011522354.1:c.258T>C	XP_011520656.1:p.Ile86=
NM_001287.6:c.432T>C MANE Select	NP_001278.1:p.Ile144=
NM_001114331.3:c.360T>C	NP_001107803.1:p.Ile120=