Canonical Allele Identifier: CA2609518421

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598423del , CM000672.2:g.70598423del GRCh38
NC_000010.10:g.72358179del , CM000672.1:g.72358179del GRCh37
NC_000010.9:g.72028185del NCBI36
NG_009615.1:g.9353del , LRG_94:g.9353del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697571.1:c.2419-465del (PALD1) ENSP00000513342.1:n.2419-465del
ENST00000697572.1:c.2250+33904del (PALD1) ENSP00000513343.1:n.2250+33904del
ENST00000697573.1:c.2263-465del (PALD1) ENSP00000513344.1:n.2263-465del
ENST00000697577.1:n.2723-465del (PALD1)
ENST00000697578.1:n.2567-465del (PALD1)
ENST00000441259.2:c.1298del (PRF1) MANE Select ENSP00000398568.1:p.Thr433MetfsTer7
ENST00000638674.1:c.540-582del (PRF1) ENSP00000492048.1:n.540-582del
ENST00000639390.1:n.98-582del (PRF1)
ENST00000373209.2:c.1298del (PRF1) ENSP00000362305.1:p.Thr433MetfsTer7
ENST00000441259.1:c.1298del (PRF1) ENSP00000398568.1:p.Thr433MetfsTer7
NM_001083116.1:c.1298del , LRG_94t1:c.1298del (PRF1) NP_001076585.1:p.Thr433MetfsTer7
NM_005041.4:c.1298del (PRF1) NP_005032.2:p.Thr433MetfsTer7
NM_001083116.2:c.1298del (PRF1) NP_001076585.1:p.Thr433MetfsTer7
NM_005041.5:c.1298del (PRF1) NP_005032.2:p.Thr433MetfsTer7
NM_001083116.3:c.1298del (PRF1) MANE Select NP_001076585.1:p.Thr433MetfsTer7
NM_005041.6:c.1298del (PRF1) NP_005032.2:p.Thr433MetfsTer7