Canonical Allele Identifier: CA998632519

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• gnomAD v3: 1-11846934-G-C
• gnomAD v4: 1-11846934-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846934G>C , CM000663.2:g.11846934G>C	GRCh38
NC_000001.10:g.11906991G>C , CM000663.1:g.11906991G>C	GRCh37
NC_000001.9:g.11829578G>C	NCBI36
NG_012926.1:g.5850C>G , LRG_751:g.5850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-643G>C (CLCN6)	ENSP00000496938.1:n.*1962-643G>C
ENST00000446542.5:n.782-500G>C (NPPA-AS1)
ENST00000376476.1:c.300+179C>G (NPPA)	ENSP00000365659.1:n.300+179C>G
ENST00000376480.7:c.450+179C>G (NPPA) MANE Select	ENSP00000365663.3:n.450+179C>G
ENST00000610706.1:c.450+179C>G (NPPA)	ENSP00000483195.1:n.450+179C>G
NM_006172.3:c.450+179C>G , LRG_751t1:c.450+179C>G (NPPA)	NP_006163.1:n.450+179C>G
NR_037806.1:n.1480-500G>C (NPPA-AS1)
NM_006172.4:c.450+179C>G (NPPA) MANE Select	NP_006163.1:n.450+179C>G