Canonical Allele Identifier: CA416362438

Linked Data

MyVariant Identifiers: chr1:g.11907503A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847446A>C , CM000663.2:g.11847446A>C GRCh38
NC_000001.10:g.11907503A>C , CM000663.1:g.11907503A>C GRCh37
NC_000001.9:g.11830090A>C NCBI36
NG_012926.1:g.5338T>G , LRG_751:g.5338T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-131A>C (CLCN6) ENSP00000496938.1:n.*1962-131A>C
ENST00000446542.5:n.794A>C (NPPA-AS1)
ENST00000376476.1:c.-27-7T>G (NPPA) ENSP00000365659.1:n.-27-7T>G
ENST00000376480.7:c.124-7T>G (NPPA) MANE Select ENSP00000365663.3:n.124-7T>G
ENST00000610706.1:c.124-7T>G (NPPA) ENSP00000483195.1:n.124-7T>G
NM_006172.3:c.124-7T>G , LRG_751t1:c.124-7T>G (NPPA) NP_006163.1:n.124-7T>G
NR_037806.1:n.1492A>C (NPPA-AS1)
NM_006172.4:c.124-7T>G (NPPA) MANE Select NP_006163.1:n.124-7T>G