Canonical Allele Identifier: CA346936896
Gene: PNPT1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.668A>T MANE Select ENSP00000400646.2:p.Lys223Ile
ENST00000260604.8:c.*223A>T ENSP00000260604.4:n.*223A>T
ENST00000415374.5:c.668A>T ENSP00000393953.1:p.Lys223Ile
ENST00000429805.1:c.*316A>T ENSP00000411994.1:n.*316A>T
ENST00000447944.6:c.668A>T ENSP00000400646.2:p.Lys223Ile
NM_033109.4:c.668A>T NP_149100.2:p.Lys223Ile
XM_005264629.1:c.428A>T XP_005264686.1:p.Lys143Ile
XM_011533142.1:c.668A>T XP_011531444.1:p.Lys223Ile
XM_005264629.2:c.428A>T XP_005264686.1:p.Lys143Ile
XM_017005172.1:c.428A>T XP_016860661.1:p.Lys143Ile
XR_001739010.1:n.698A>T
NM_033109.5:c.668A>T MANE Select NP_149100.2:p.Lys223Ile