Canonical Allele Identifier: CA2659134420
Gene: PNPT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55680982del , CM000664.2:g.55680982del GRCh38
NC_000002.11:g.55908117del , CM000664.1:g.55908117del GRCh37
NC_000002.10:g.55761621del NCBI36
NG_033012.1:g.17932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000447944.7:c.454-61del MANE Select ENSP00000400646.2:n.454-61del
ENST00000260604.8:c.454-61del ENSP00000260604.4:n.454-61del
ENST00000415374.5:c.454-61del ENSP00000393953.1:n.454-61del
ENST00000429805.1:c.*102-61del ENSP00000411994.1:n.*102-61del
ENST00000447944.6:c.454-61del ENSP00000400646.2:n.454-61del
NM_033109.4:c.454-61del NP_149100.2:n.454-61del
XM_005264629.1:c.214-61del XP_005264686.1:n.214-61del
XM_011533142.1:c.454-61del XP_011531444.1:n.454-61del
XM_005264629.2:c.214-61del XP_005264686.1:n.214-61del
XM_017005172.1:c.214-61del XP_016860661.1:n.214-61del
XR_001739010.1:n.484-61del
NM_033109.5:c.454-61del MANE Select NP_149100.2:n.454-61del