Canonical Allele Identifier: CA2574215289

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• ClinVar Variation Id: 2179668
• ClinVar RCV Id: RCV002615180
• gnomAD v4: 1-11846030-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846030A>G , CM000663.2:g.11846030A>G	GRCh38
NC_000001.10:g.11906087A>G , CM000663.1:g.11906087A>G	GRCh37
NC_000001.9:g.11828674A>G	NCBI36
NG_012926.1:g.6754T>C , LRG_751:g.6754T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400892.3:c.*1961+264A>G (CLCN6)	ENSP00000496938.1:n.*1961+264A>G
ENST00000446542.5:n.781+264A>G (NPPA-AS1)
ENST00000376476.1:c.301-16T>C (NPPA)	ENSP00000365659.1:n.301-16T>C
ENST00000376480.7:c.451-16T>C (NPPA) MANE Select	ENSP00000365663.3:n.451-16T>C
ENST00000610706.1:c.451-16T>C (NPPA)	ENSP00000483195.1:n.451-16T>C
NM_006172.3:c.451-16T>C , LRG_751t1:c.451-16T>C (NPPA)	NP_006163.1:n.451-16T>C
NR_037806.1:n.1479+264A>G (NPPA-AS1)
NM_006172.4:c.451-16T>C (NPPA) MANE Select	NP_006163.1:n.451-16T>C