Canonical Allele Identifier: CA1153831613

Linked Data

dbSNP Id: rs564275613

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846974G>A , CM000663.2:g.11846974G>A GRCh38
NC_000001.10:g.11907031G>A , CM000663.1:g.11907031G>A GRCh37
NC_000001.9:g.11829618G>A NCBI36
NG_012926.1:g.5810C>T , LRG_751:g.5810C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-603G>A (CLCN6) ENSP00000496938.1:n.*1962-603G>A
ENST00000446542.5:n.782-460G>A (NPPA-AS1)
ENST00000376476.1:c.300+139C>T (NPPA) ENSP00000365659.1:n.300+139C>T
ENST00000376480.7:c.450+139C>T (NPPA) MANE Select ENSP00000365663.3:n.450+139C>T
ENST00000610706.1:c.450+139C>T (NPPA) ENSP00000483195.1:n.450+139C>T
NM_006172.3:c.450+139C>T , LRG_751t1:c.450+139C>T (NPPA) NP_006163.1:n.450+139C>T
NR_037806.1:n.1480-460G>A (NPPA-AS1)
NM_006172.4:c.450+139C>T (NPPA) MANE Select NP_006163.1:n.450+139C>T