Canonical Allele Identifier: CA1153830324

Linked Data

dbSNP Id: rs1645067125

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846192del , CM000663.2:g.11846192del GRCh38
NC_000001.10:g.11906249del , CM000663.1:g.11906249del GRCh37
NC_000001.9:g.11828836del NCBI36
NG_012926.1:g.6592del , LRG_751:g.6592del

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+426del (CLCN6) ENSP00000496938.1:n.*1961+426del
ENST00000446542.5:n.781+426del (NPPA-AS1)
ENST00000376476.1:c.301-178del (NPPA) ENSP00000365659.1:n.301-178del
ENST00000376480.7:c.451-178del (NPPA) MANE Select ENSP00000365663.3:n.451-178del
ENST00000610706.1:c.451-178del (NPPA) ENSP00000483195.1:n.451-178del
NM_006172.3:c.451-178del , LRG_751t1:c.451-178del (NPPA) NP_006163.1:n.451-178del
NR_037806.1:n.1479+426del (NPPA-AS1)
NM_006172.4:c.451-178del (NPPA) MANE Select NP_006163.1:n.451-178del