Canonical Allele Identifier: CA394185723

Gene: CLCN7

Linked Data

• MyVariant Identifiers: chr16:g.1497517T>C (hg19) ; chr16:g.1447516T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447516T>C , CM000678.2:g.1447516T>C	GRCh38
NC_000016.9:g.1497517T>C , CM000678.1:g.1497517T>C	GRCh37
NC_000016.8:g.1437518T>C	NCBI36
NG_007567.1:g.32569A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2126A>G	ENSP00000514703.1:p.Lys709Arg
ENST00000699948.1:c.*439A>G	ENSP00000514704.1:n.*439A>G
ENST00000382745.9:c.2126A>G MANE Select	ENSP00000372193.4:p.Lys709Arg
ENST00000262318.12:c.2054A>G	ENSP00000262318.8:p.Lys685Arg
ENST00000382745.8:c.2126A>G	ENSP00000372193.4:p.Lys709Arg
ENST00000448525.5:c.2054A>G	ENSP00000410907.1:p.Lys685Arg
ENST00000563642.6:n.2195A>G
ENST00000565092.6:n.1161A>G
ENST00000567836.2:n.367A>G
NM_001114331.2:c.2054A>G	NP_001107803.1:p.Lys685Arg
NM_001287.5:c.2126A>G	NP_001278.1:p.Lys709Arg
XM_011522354.1:c.1952A>G	XP_011520656.1:p.Lys651Arg
NM_001287.6:c.2126A>G MANE Select	NP_001278.1:p.Lys709Arg
NM_001114331.3:c.2054A>G	NP_001107803.1:p.Lys685Arg