Canonical Allele Identifier: CA2580090690

Gene: CLCN7

Linked Data

• ClinVar Variation Id: 2098828
• ClinVar RCV Id: RCV003031138

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1449106T>A , CM000678.2:g.1449106T>A	GRCh38
NC_000016.9:g.1499107T>A , CM000678.1:g.1499107T>A	GRCh37
NC_000016.8:g.1439108T>A	NCBI36
NG_007567.1:g.30979A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.1670-13A>T	ENSP00000514703.1:n.1670-13A>T
ENST00000699948.1:c.1624-13A>T	ENSP00000514704.1:n.1624-13A>T
ENST00000382745.9:c.1670-13A>T MANE Select	ENSP00000372193.4:n.1670-13A>T
ENST00000262318.12:c.1598-13A>T	ENSP00000262318.8:n.1598-13A>T
ENST00000382745.8:c.1670-13A>T	ENSP00000372193.4:n.1670-13A>T
ENST00000448525.5:c.1598-13A>T	ENSP00000410907.1:n.1598-13A>T
ENST00000563642.6:n.1739-13A>T
ENST00000565092.6:n.692A>T
ENST00000567789.1:n.158A>T
NM_001114331.2:c.1598-13A>T	NP_001107803.1:n.1598-13A>T
NM_001287.5:c.1670-13A>T	NP_001278.1:n.1670-13A>T
XM_011522354.1:c.1496-13A>T	XP_011520656.1:n.1496-13A>T
NM_001287.6:c.1670-13A>T MANE Select	NP_001278.1:n.1670-13A>T
NM_001114331.3:c.1598-13A>T	NP_001107803.1:n.1598-13A>T