Canonical Allele Identifier: CA18010464

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• dbSNP Id: rs901329482
• MyVariant Identifiers: chr1:g.11907026G>A (hg19) ; chr1:g.11846969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846969G>A , CM000663.2:g.11846969G>A	GRCh38
NC_000001.10:g.11907026G>A , CM000663.1:g.11907026G>A	GRCh37
NC_000001.9:g.11829613G>A	NCBI36
NG_012926.1:g.5815C>T , LRG_751:g.5815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-608G>A (CLCN6)	ENSP00000496938.1:n.*1962-608G>A
ENST00000446542.5:n.782-465G>A (NPPA-AS1)
ENST00000376476.1:c.300+144C>T (NPPA)	ENSP00000365659.1:n.300+144C>T
ENST00000376480.7:c.450+144C>T (NPPA) MANE Select	ENSP00000365663.3:n.450+144C>T
ENST00000610706.1:c.450+144C>T (NPPA)	ENSP00000483195.1:n.450+144C>T
NM_006172.3:c.450+144C>T , LRG_751t1:c.450+144C>T (NPPA)	NP_006163.1:n.450+144C>T
NR_037806.1:n.1480-465G>A (NPPA-AS1)
NM_006172.4:c.450+144C>T (NPPA) MANE Select	NP_006163.1:n.450+144C>T