Canonical Allele Identifier: CA916109099

Linked Data

dbSNP Id: rs1553123090

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847591_11847602dup , CM000663.2:g.11847591_11847602dup GRCh38
NC_000001.10:g.11907648_11907659dup , CM000663.1:g.11907648_11907659dup GRCh37
NC_000001.9:g.11830235_11830246dup NCBI36
NG_012926.1:g.5185_5196dup , LRG_751:g.5185_5196dup

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1976_*1987dup (CLCN6) ENSP00000496938.1:n.*1976_*1987dup
ENST00000446542.5:n.939_950dup (NPPA-AS1)
ENST00000376476.1:c.-27-160_-27-149dup (NPPA) ENSP00000365659.1:n.-27-160_-27-149dup
ENST00000376480.7:c.86_97dup (NPPA) MANE Select ENSP00000365663.3:p.Val32_Ser33insTyrAsnA...
ENST00000610706.1:c.86_97dup (NPPA) ENSP00000483195.1:p.Val32_Ser33insTyrAsnA...
NM_006172.3:c.86_97dup , LRG_751t1:c.86_97dup (NPPA) NP_006163.1:p.Val32_Ser33insTyrAsnAlaVal
NR_037806.1:n.1637_1648dup (NPPA-AS1)
NM_006172.4:c.86_97dup (NPPA) MANE Select NP_006163.1:p.Val32_Ser33insTyrAsnAlaVal