Canonical Allele Identifier: CA1252405128
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55679712C= , CM000664.2:g.55679712C= GRCh38
NC_000002.11:g.55906847C= , CM000664.1:g.55906847C= GRCh37
NC_000002.10:g.55760351C= NCBI36
NG_033012.1:g.19199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447944.7:c.649G= MANE Select ENSP00000400646.2:p.Val217=
ENST00000260604.8:c.*204G= ENSP00000260604.4:n.*204G=
ENST00000415374.5:c.649G= ENSP00000393953.1:p.Val217=
ENST00000429805.1:c.*297G= ENSP00000411994.1:n.*297G=
ENST00000447944.6:c.649G= ENSP00000400646.2:p.Val217=
NM_033109.4:c.649G= NP_149100.2:p.Val217=
XM_005264629.1:c.409G= XP_005264686.1:p.Val137=
XM_011533142.1:c.649G= XP_011531444.1:p.Val217=
XM_005264629.2:c.409G= XP_005264686.1:p.Val137=
XM_017005172.1:c.409G= XP_016860661.1:p.Val137=
XR_001739010.1:n.679G=
NM_033109.5:c.649G= MANE Select NP_149100.2:p.Val217=