Canonical Allele Identifier: CA1252401121
Gene: PNPT1 HGNC NCBI

Linked Data

dbSNP Id: rs1696936611

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55672156_55672159del , CM000664.2:g.55672156_55672159del GRCh38
NC_000002.11:g.55899291_55899294del , CM000664.1:g.55899291_55899294del GRCh37
NC_000002.10:g.55752795_55752798del NCBI36
NG_033012.1:g.26756_26759del

Transcript Alleles

HGVS Amino-acid Change
ENST00000447944.7:c.867-109_867-106del MANE Select ENSP00000400646.2:n.867-109_867-106del
ENST00000260604.8:c.*422-109_*422-106del ENSP00000260604.4:n.*422-109_*422-106del
ENST00000415374.5:c.867-109_867-106del ENSP00000393953.1:n.867-109_867-106del
ENST00000447944.6:c.867-109_867-106del ENSP00000400646.2:n.867-109_867-106del
NM_033109.4:c.867-109_867-106del NP_149100.2:n.867-109_867-106del
XM_005264629.1:c.627-109_627-106del XP_005264686.1:n.627-109_627-106del
XM_011533142.1:c.867-109_867-106del XP_011531444.1:n.867-109_867-106del
XM_005264629.2:c.627-109_627-106del XP_005264686.1:n.627-109_627-106del
XM_017005172.1:c.627-109_627-106del XP_016860661.1:n.627-109_627-106del
XR_001739010.1:n.897-109_897-106del
NM_033109.5:c.867-109_867-106del MANE Select NP_149100.2:n.867-109_867-106del