Canonical Allele Identifier: CA998632604

Linked Data

dbSNP Id: rs1645073826

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847084_11847099del , CM000663.2:g.11847084_11847099del GRCh38
NC_000001.10:g.11907141_11907156del , CM000663.1:g.11907141_11907156del GRCh37
NC_000001.9:g.11829728_11829743del NCBI36
NG_012926.1:g.5693_5708del , LRG_751:g.5693_5708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-493_*1962-478del (CLCN6) ENSP00000496938.1:n.*1962-493_*1962-478del
ENST00000446542.5:n.782-350_782-335del (NPPA-AS1)
ENST00000376476.1:c.300+22_300+37del (NPPA) ENSP00000365659.1:n.300+22_300+37del
ENST00000376480.7:c.450+22_450+37del (NPPA) MANE Select ENSP00000365663.3:n.450+22_450+37del
ENST00000610706.1:c.450+22_450+37del (NPPA) ENSP00000483195.1:n.450+22_450+37del
NM_006172.3:c.450+22_450+37del , LRG_751t1:c.450+22_450+37del (NPPA) NP_006163.1:n.450+22_450+37del
NR_037806.1:n.1480-350_1480-335del (NPPA-AS1)
NM_006172.4:c.450+22_450+37del (NPPA) MANE Select NP_006163.1:n.450+22_450+37del