Canonical Allele Identifier: CA2122043927

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472469G= , CM000676.2:g.20472469G=	GRCh38
NC_000014.8:g.20940628G= , CM000676.1:g.20940628G=	GRCh37
NC_000014.7:g.20010468G=	NCBI36
NG_009631.1:g.8087G= , LRG_91:g.8087G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.290G=	ENSP00000452421.2:p.Arg97=
ENST00000556293.6:n.292G=
ENST00000556754.2:n.1235G=
ENST00000557229.6:n.292G=
ENST00000697613.1:c.173G=	ENSP00000513359.1:p.Arg58=
ENST00000697614.1:c.-65G=	ENSP00000513360.1:n.-65G=
ENST00000697615.1:n.691G=
ENST00000361505.10:c.173G= MANE Select	ENSP00000354532.6:p.Arg58=
ENST00000361505.9:c.173G=	ENSP00000354532.5:p.Arg58=
ENST00000553418.5:c.173G=	ENSP00000450663.1:p.Arg58=
ENST00000553591.1:c.290G=	ENSP00000452421.1:p.Arg97=
ENST00000554056.5:n.284G=
ENST00000554065.1:c.-65G=	ENSP00000451108.1:n.-65G=
ENST00000556293.5:n.292G=
ENST00000557229.5:n.292G=
NM_000270.3:c.173G= , LRG_91t1:c.173G=	NP_000261.2:p.Arg58=
NM_000270.4:c.173G= MANE Select	NP_000261.2:p.Arg58=