Canonical Allele Identifier: CA2643312124

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847513_11847518del , CM000663.2:g.11847513_11847518del GRCh38
NC_000001.10:g.11907570_11907575del , CM000663.1:g.11907570_11907575del GRCh37
NC_000001.9:g.11830157_11830162del NCBI36
NG_012926.1:g.5269_5274del , LRG_751:g.5269_5274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-64_*1962-59del (CLCN6) ENSP00000496938.1:n.*1962-64_*1962-59del
ENST00000446542.5:n.861_866del (NPPA-AS1)
ENST00000376476.1:c.-27-76_-27-71del (NPPA) ENSP00000365659.1:n.-27-76_-27-71del
ENST00000376480.7:c.123+47_123+52del (NPPA) MANE Select ENSP00000365663.3:n.123+47_123+52del
ENST00000610706.1:c.123+47_123+52del (NPPA) ENSP00000483195.1:n.123+47_123+52del
NM_006172.3:c.123+47_123+52del , LRG_751t1:c.123+47_123+52del (NPPA) NP_006163.1:n.123+47_123+52del
NR_037806.1:n.1559_1564del (NPPA-AS1)
NM_006172.4:c.123+47_123+52del (NPPA) MANE Select NP_006163.1:n.123+47_123+52del