Canonical Allele Identifier: CA1252384381
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55643263A= , CM000664.2:g.55643263A= GRCh38
NC_000002.11:g.55870398A= , CM000664.1:g.55870398A= GRCh37
NC_000002.10:g.55723902A= NCBI36
NG_033012.1:g.55648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447944.7:c.2014-50T= MANE Select ENSP00000400646.2:n.2014-50T=
ENST00000260604.8:c.*1556-50T= ENSP00000260604.4:n.*1556-50T=
ENST00000415374.5:c.2014-50T= ENSP00000393953.1:n.2014-50T=
ENST00000447944.6:c.2014-50T= ENSP00000400646.2:n.2014-50T=
ENST00000481066.1:n.1076-50T=
NM_033109.4:c.2014-50T= NP_149100.2:n.2014-50T=
XM_005264629.1:c.1774-50T= XP_005264686.1:n.1774-50T=
XM_005264629.2:c.1774-50T= XP_005264686.1:n.1774-50T=
XM_017005172.1:c.1774-50T= XP_016860661.1:n.1774-50T=
NM_033109.5:c.2014-50T= MANE Select NP_149100.2:n.2014-50T=