Canonical Allele Identifier: CA521455488

Linked Data

dbSNP Id: rs1213644227

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847455dup , CM000663.2:g.11847455dup GRCh38
NC_000001.10:g.11907512dup , CM000663.1:g.11907512dup GRCh37
NC_000001.9:g.11830099dup NCBI36
NG_012926.1:g.5332dup , LRG_751:g.5332dup

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-122dup (CLCN6) ENSP00000496938.1:n.*1962-122dup
ENST00000446542.5:n.803dup (NPPA-AS1)
ENST00000376476.1:c.-27-13dup (NPPA) ENSP00000365659.1:n.-27-13dup
ENST00000376480.7:c.124-13dup (NPPA) MANE Select ENSP00000365663.3:n.124-13dup
ENST00000610706.1:c.124-13dup (NPPA) ENSP00000483195.1:n.124-13dup
NM_006172.3:c.124-13dup , LRG_751t1:c.124-13dup (NPPA) NP_006163.1:n.124-13dup
NR_037806.1:n.1501dup (NPPA-AS1)
NM_006172.4:c.124-13dup (NPPA) MANE Select NP_006163.1:n.124-13dup