Canonical Allele Identifier: CA18010141

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• dbSNP Id: rs981977158
• gnomAD v3: 1-11846194-A-C
• gnomAD v4: 1-11846194-A-C
• MyVariant Identifiers: chr1:g.11906251A>C (hg19) ; chr1:g.11846194A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846194A>C , CM000663.2:g.11846194A>C	GRCh38
NC_000001.10:g.11906251A>C , CM000663.1:g.11906251A>C	GRCh37
NC_000001.9:g.11828838A>C	NCBI36
NG_012926.1:g.6590T>G , LRG_751:g.6590T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400892.3:c.*1961+428A>C (CLCN6)	ENSP00000496938.1:n.*1961+428A>C
ENST00000446542.5:n.781+428A>C (NPPA-AS1)
ENST00000376476.1:c.301-180T>G (NPPA)	ENSP00000365659.1:n.301-180T>G
ENST00000376480.7:c.451-180T>G (NPPA) MANE Select	ENSP00000365663.3:n.451-180T>G
ENST00000610706.1:c.451-180T>G (NPPA)	ENSP00000483195.1:n.451-180T>G
NM_006172.3:c.451-180T>G , LRG_751t1:c.451-180T>G (NPPA)	NP_006163.1:n.451-180T>G
NR_037806.1:n.1479+428A>C (NPPA-AS1)
NM_006172.4:c.451-180T>G (NPPA) MANE Select	NP_006163.1:n.451-180T>G