Canonical Allele Identifier: CA2122045168
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20475197C= , CM000676.2:g.20475197C= GRCh38
NC_000014.8:g.20943356C= , CM000676.1:g.20943356C= GRCh37
NC_000014.7:g.20013196C= NCBI36
NG_009631.1:g.10815C= , LRG_91:g.10815C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553591.2:c.714C= ENSP00000452421.2:p.Ser238=
ENST00000556293.6:n.3020C=
ENST00000556754.2:n.3963C=
ENST00000557229.6:n.1026C=
ENST00000697613.1:c.597C= ENSP00000513359.1:p.Ser199=
ENST00000697614.1:c.360C= ENSP00000513360.1:p.Ser120=
ENST00000697615.1:n.1425C=
ENST00000361505.10:c.597C= MANE Select ENSP00000354532.6:p.Ser199=
ENST00000361505.9:c.597C= ENSP00000354532.5:p.Ser199=
ENST00000554056.5:n.905C=
ENST00000556754.1:n.1814C=
NM_000270.3:c.597C= , LRG_91t1:c.597C= NP_000261.2:p.Ser199=
NM_000270.4:c.597C= MANE Select NP_000261.2:p.Ser199=