Canonical Allele Identifier: CA2122043861
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20472301C= , CM000676.2:g.20472301C= GRCh38
NC_000014.8:g.20940460C= , CM000676.1:g.20940460C= GRCh37
NC_000014.7:g.20010300C= NCBI36
NG_009631.1:g.7919C= , LRG_91:g.7919C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553591.2:c.129-7C= ENSP00000452421.2:n.129-7C=
ENST00000556293.6:n.131-7C=
ENST00000556754.2:n.1067C=
ENST00000557229.6:n.131-7C=
ENST00000697613.1:c.12-7C= ENSP00000513359.1:n.12-7C=
ENST00000697614.1:c.-226-7C= ENSP00000513360.1:n.-226-7C=
ENST00000697615.1:n.523C=
ENST00000361505.10:c.12-7C= MANE Select ENSP00000354532.6:n.12-7C=
ENST00000361505.9:c.12-7C= ENSP00000354532.5:n.12-7C=
ENST00000553418.5:c.12-7C= ENSP00000450663.1:n.12-7C=
ENST00000553591.1:c.129-7C= ENSP00000452421.1:n.129-7C=
ENST00000554056.5:n.123-7C=
ENST00000554065.1:c.-226-7C= ENSP00000451108.1:n.-226-7C=
ENST00000556293.5:n.131-7C=
ENST00000557229.5:n.131-7C=
NM_000270.3:c.12-7C= , LRG_91t1:c.12-7C= NP_000261.2:n.12-7C=
NM_000270.4:c.12-7C= MANE Select NP_000261.2:n.12-7C=