Canonical Allele Identifier: CA394185409

Gene: CLCN7

Linked Data

• MyVariant Identifiers: chr16:g.1497081A>T (hg19) ; chr16:g.1447080A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447080A>T , CM000678.2:g.1447080A>T	GRCh38
NC_000016.9:g.1497081A>T , CM000678.1:g.1497081A>T	GRCh37
NC_000016.8:g.1437082A>T	NCBI36
NG_007567.1:g.33005T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2257T>A	ENSP00000514703.1:p.Ser753Thr
ENST00000699948.1:c.*570T>A	ENSP00000514704.1:n.*570T>A
ENST00000382745.9:c.2257T>A MANE Select	ENSP00000372193.4:p.Ser753Thr
ENST00000262318.12:c.2186T>A	ENSP00000262318.8:p.Val729Asp
ENST00000382745.8:c.2257T>A	ENSP00000372193.4:p.Ser753Thr
ENST00000448525.5:c.2185T>A	ENSP00000410907.1:p.Ser729Thr
ENST00000563642.6:n.2326T>A
ENST00000565092.6:n.1292T>A
ENST00000567836.2:n.498T>A
NM_001114331.2:c.2185T>A	NP_001107803.1:p.Ser729Thr
NM_001287.5:c.2257T>A	NP_001278.1:p.Ser753Thr
XM_011522354.1:c.2083T>A	XP_011520656.1:p.Ser695Thr
NM_001287.6:c.2257T>A MANE Select	NP_001278.1:p.Ser753Thr
NM_001114331.3:c.2185T>A	NP_001107803.1:p.Ser729Thr