Canonical Allele Identifier: CA2643311586

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847086_11847090del , CM000663.2:g.11847086_11847090del GRCh38
NC_000001.10:g.11907143_11907147del , CM000663.1:g.11907143_11907147del GRCh37
NC_000001.9:g.11829730_11829734del NCBI36
NG_012926.1:g.5703_5707del , LRG_751:g.5703_5707del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-491_*1962-487del (CLCN6) ENSP00000496938.1:n.*1962-491_*1962-487del
ENST00000446542.5:n.782-348_782-344del (NPPA-AS1)
ENST00000376476.1:c.300+32_300+36del (NPPA) ENSP00000365659.1:n.300+32_300+36del
ENST00000376480.7:c.450+32_450+36del (NPPA) MANE Select ENSP00000365663.3:n.450+32_450+36del
ENST00000610706.1:c.450+32_450+36del (NPPA) ENSP00000483195.1:n.450+32_450+36del
NM_006172.3:c.450+32_450+36del , LRG_751t1:c.450+32_450+36del (NPPA) NP_006163.1:n.450+32_450+36del
NR_037806.1:n.1480-348_1480-344del (NPPA-AS1)
NM_006172.4:c.450+32_450+36del (NPPA) MANE Select NP_006163.1:n.450+32_450+36del