Canonical Allele Identifier: CA2122043894
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20472366C= , CM000676.2:g.20472366C= GRCh38
NC_000014.8:g.20940525C= , CM000676.1:g.20940525C= GRCh37
NC_000014.7:g.20010365C= NCBI36
NG_009631.1:g.7984C= , LRG_91:g.7984C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553591.2:c.187C= ENSP00000452421.2:p.Arg63=
ENST00000556293.6:n.189C=
ENST00000556754.2:n.1132C=
ENST00000557229.6:n.189C=
ENST00000697613.1:c.70C= ENSP00000513359.1:p.Arg24=
ENST00000697614.1:c.-168C= ENSP00000513360.1:n.-168C=
ENST00000697615.1:n.588C=
ENST00000361505.10:c.70C= MANE Select ENSP00000354532.6:p.Arg24=
ENST00000361505.9:c.70C= ENSP00000354532.5:p.Arg24=
ENST00000553418.5:c.70C= ENSP00000450663.1:p.Arg24=
ENST00000553591.1:c.187C= ENSP00000452421.1:p.Arg63=
ENST00000554056.5:n.181C=
ENST00000554065.1:c.-168C= ENSP00000451108.1:n.-168C=
ENST00000556293.5:n.189C=
ENST00000557229.5:n.189C=
NM_000270.3:c.70C= , LRG_91t1:c.70C= NP_000261.2:p.Arg24=
NM_000270.4:c.70C= MANE Select NP_000261.2:p.Arg24=