Canonical Allele Identifier: CA886104937

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• dbSNP Id: rs1340134586
• gnomAD v3: 1-11846830-A-G
• gnomAD v4: 1-11846830-A-G
• MyVariant Identifiers: chr1:g.11906887A>G (hg19) ; chr1:g.11846830A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846830A>G , CM000663.2:g.11846830A>G	GRCh38
NC_000001.10:g.11906887A>G , CM000663.1:g.11906887A>G	GRCh37
NC_000001.9:g.11829474A>G	NCBI36
NG_012926.1:g.5954T>C , LRG_751:g.5954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-747A>G (CLCN6)	ENSP00000496938.1:n.*1962-747A>G
ENST00000446542.5:n.782-604A>G (NPPA-AS1)
ENST00000376476.1:c.300+283T>C (NPPA)	ENSP00000365659.1:n.300+283T>C
ENST00000376480.7:c.450+283T>C (NPPA) MANE Select	ENSP00000365663.3:n.450+283T>C
ENST00000610706.1:c.450+283T>C (NPPA)	ENSP00000483195.1:n.450+283T>C
NM_006172.3:c.450+283T>C , LRG_751t1:c.450+283T>C (NPPA)	NP_006163.1:n.450+283T>C
NR_037806.1:n.1480-604A>G (NPPA-AS1)
NM_006172.4:c.450+283T>C (NPPA) MANE Select	NP_006163.1:n.450+283T>C