Canonical Allele Identifier: CA2122043897
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20472371T= , CM000676.2:g.20472371T= GRCh38
NC_000014.8:g.20940530T= , CM000676.1:g.20940530T= GRCh37
NC_000014.7:g.20010370T= NCBI36
NG_009631.1:g.7989T= , LRG_91:g.7989T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553591.2:c.192T= ENSP00000452421.2:p.Pro64=
ENST00000556293.6:n.194T=
ENST00000556754.2:n.1137T=
ENST00000557229.6:n.194T=
ENST00000697613.1:c.75T= ENSP00000513359.1:p.Pro25=
ENST00000697614.1:c.-163T= ENSP00000513360.1:n.-163T=
ENST00000697615.1:n.593T=
ENST00000361505.10:c.75T= MANE Select ENSP00000354532.6:p.Pro25=
ENST00000361505.9:c.75T= ENSP00000354532.5:p.Pro25=
ENST00000553418.5:c.75T= ENSP00000450663.1:p.Pro25=
ENST00000553591.1:c.192T= ENSP00000452421.1:p.Pro64=
ENST00000554056.5:n.186T=
ENST00000554065.1:c.-163T= ENSP00000451108.1:n.-163T=
ENST00000556293.5:n.194T=
ENST00000557229.5:n.194T=
NM_000270.3:c.75T= , LRG_91t1:c.75T= NP_000261.2:p.Pro25=
NM_000270.4:c.75T= MANE Select NP_000261.2:p.Pro25=