Canonical Allele Identifier: CA998632156

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• dbSNP Id: rs1645071092
• gnomAD v3: 1-11846702-GC-G
• gnomAD v4: 1-11846702-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846704del , CM000663.2:g.11846704del	GRCh38
NC_000001.10:g.11906761del , CM000663.1:g.11906761del	GRCh37
NC_000001.9:g.11829348del	NCBI36
NG_012926.1:g.6081del , LRG_751:g.6081del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-873del (CLCN6)	ENSP00000496938.1:n.*1962-873del
ENST00000446542.5:n.782-730del (NPPA-AS1)
ENST00000376476.1:c.300+410del (NPPA)	ENSP00000365659.1:n.300+410del
ENST00000376480.7:c.450+410del (NPPA) MANE Select	ENSP00000365663.3:n.450+410del
ENST00000610706.1:c.450+410del (NPPA)	ENSP00000483195.1:n.450+410del
NM_006172.3:c.450+410del , LRG_751t1:c.450+410del (NPPA)	NP_006163.1:n.450+410del
NR_037806.1:n.1480-730del (NPPA-AS1)
NM_006172.4:c.450+410del (NPPA) MANE Select	NP_006163.1:n.450+410del