Canonical Allele Identifier: CA1252405123
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55679693T= , CM000664.2:g.55679693T= GRCh38
NC_000002.11:g.55906828T= , CM000664.1:g.55906828T= GRCh37
NC_000002.10:g.55760332T= NCBI36
NG_033012.1:g.19218A=

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.668A= MANE Select ENSP00000400646.2:p.Lys223=
ENST00000260604.8:c.*223A= ENSP00000260604.4:n.*223A=
ENST00000415374.5:c.668A= ENSP00000393953.1:p.Lys223=
ENST00000429805.1:c.*316A= ENSP00000411994.1:n.*316A=
ENST00000447944.6:c.668A= ENSP00000400646.2:p.Lys223=
NM_033109.4:c.668A= NP_149100.2:p.Lys223=
XM_005264629.1:c.428A= XP_005264686.1:p.Lys143=
XM_011533142.1:c.668A= XP_011531444.1:p.Lys223=
XM_005264629.2:c.428A= XP_005264686.1:p.Lys143=
XM_017005172.1:c.428A= XP_016860661.1:p.Lys143=
XR_001739010.1:n.698A=
NM_033109.5:c.668A= MANE Select NP_149100.2:p.Lys223=