Canonical Allele Identifier: CA1252384287
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55643182T= , CM000664.2:g.55643182T= GRCh38
NC_000002.11:g.55870317T= , CM000664.1:g.55870317T= GRCh37
NC_000002.10:g.55723821T= NCBI36
NG_033012.1:g.55729A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447944.7:c.2045A= MANE Select ENSP00000400646.2:p.Tyr682=
ENST00000260604.8:c.*1587A= ENSP00000260604.4:n.*1587A=
ENST00000415374.5:c.2045A= ENSP00000393953.1:p.Tyr682=
ENST00000447944.6:c.2045A= ENSP00000400646.2:p.Tyr682=
ENST00000481066.1:n.1107A=
NM_033109.4:c.2045A= NP_149100.2:p.Tyr682=
XM_005264629.1:c.1805A= XP_005264686.1:p.Tyr602=
XM_005264629.2:c.1805A= XP_005264686.1:p.Tyr602=
XM_017005172.1:c.1805A= XP_016860661.1:p.Tyr602=
NM_033109.5:c.2045A= MANE Select NP_149100.2:p.Tyr682=