Canonical Allele Identifier: CA2122043866
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20472309T= , CM000676.2:g.20472309T= GRCh38
NC_000014.8:g.20940468T= , CM000676.1:g.20940468T= GRCh37
NC_000014.7:g.20010308T= NCBI36
NG_009631.1:g.7927T= , LRG_91:g.7927T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553591.2:c.130T= ENSP00000452421.2:p.Tyr44=
ENST00000556293.6:n.132T=
ENST00000556754.2:n.1075T=
ENST00000557229.6:n.132T=
ENST00000697613.1:c.13T= ENSP00000513359.1:p.Tyr5=
ENST00000697614.1:c.-225T= ENSP00000513360.1:n.-225T=
ENST00000697615.1:n.531T=
ENST00000361505.10:c.13T= MANE Select ENSP00000354532.6:p.Tyr5=
ENST00000361505.9:c.13T= ENSP00000354532.5:p.Tyr5=
ENST00000553418.5:c.13T= ENSP00000450663.1:p.Tyr5=
ENST00000553591.1:c.130T= ENSP00000452421.1:p.Tyr44=
ENST00000554056.5:n.124T=
ENST00000554065.1:c.-225T= ENSP00000451108.1:n.-225T=
ENST00000556293.5:n.132T=
ENST00000557229.5:n.132T=
NM_000270.3:c.13T= , LRG_91t1:c.13T= NP_000261.2:p.Tyr5=
NM_000270.4:c.13T= MANE Select NP_000261.2:p.Tyr5=