Canonical Allele Identifier: CA2643311282

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846136_11846155del , CM000663.2:g.11846136_11846155del GRCh38
NC_000001.10:g.11906193_11906212del , CM000663.1:g.11906193_11906212del GRCh37
NC_000001.9:g.11828780_11828799del NCBI36
NG_012926.1:g.6632_6651del , LRG_751:g.6632_6651del

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+370_*1961+389del (CLCN6) ENSP00000496938.1:n.*1961+370_*1961+389de...
ENST00000446542.5:n.781+370_781+389del (NPPA-AS1)
ENST00000376476.1:c.301-138_301-119del (NPPA) ENSP00000365659.1:n.301-138_301-119del
ENST00000376480.7:c.451-138_451-119del (NPPA) MANE Select ENSP00000365663.3:n.451-138_451-119del
ENST00000610706.1:c.451-138_451-119del (NPPA) ENSP00000483195.1:n.451-138_451-119del
NM_006172.3:c.451-138_451-119del , LRG_751t1:c.451-138_451-119del (NPPA) NP_006163.1:n.451-138_451-119del
NR_037806.1:n.1479+370_1479+389del (NPPA-AS1)
NM_006172.4:c.451-138_451-119del (NPPA) MANE Select NP_006163.1:n.451-138_451-119del