Canonical Allele Identifier: CA1252398320
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55666914T= , CM000664.2:g.55666914T= GRCh38
NC_000002.11:g.55894049T= , CM000664.1:g.55894049T= GRCh37
NC_000002.10:g.55747553T= NCBI36
NG_033012.1:g.31997A=

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.1176+77A= MANE Select ENSP00000400646.2:n.1176+77A=
ENST00000260604.8:c.*731+77A= ENSP00000260604.4:n.*731+77A=
ENST00000415374.5:c.1176+77A= ENSP00000393953.1:n.1176+77A=
ENST00000415489.1:c.250+77A=
ENST00000447944.6:c.1176+77A= ENSP00000400646.2:n.1176+77A=
NM_033109.4:c.1176+77A= NP_149100.2:n.1176+77A=
XM_005264629.1:c.936+77A= XP_005264686.1:n.936+77A=
XM_011533142.1:c.1176+77A= XP_011531444.1:n.1176+77A=
XM_005264629.2:c.936+77A= XP_005264686.1:n.936+77A=
XM_017005172.1:c.936+77A= XP_016860661.1:n.936+77A=
XR_001739010.1:n.1206+77A=
NM_033109.5:c.1176+77A= MANE Select NP_149100.2:n.1176+77A=