Canonical Allele Identifier: CA2122043863
Gene: PNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20472303C= , CM000676.2:g.20472303C= GRCh38
NC_000014.8:g.20940462C= , CM000676.1:g.20940462C= GRCh37
NC_000014.7:g.20010302C= NCBI36
NG_009631.1:g.7921C= , LRG_91:g.7921C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553591.2:c.129-5C= ENSP00000452421.2:n.129-5C=
ENST00000556293.6:n.131-5C=
ENST00000556754.2:n.1069C=
ENST00000557229.6:n.131-5C=
ENST00000697613.1:c.12-5C= ENSP00000513359.1:n.12-5C=
ENST00000697614.1:c.-226-5C= ENSP00000513360.1:n.-226-5C=
ENST00000697615.1:n.525C=
ENST00000361505.10:c.12-5C= MANE Select ENSP00000354532.6:n.12-5C=
ENST00000361505.9:c.12-5C= ENSP00000354532.5:n.12-5C=
ENST00000553418.5:c.12-5C= ENSP00000450663.1:n.12-5C=
ENST00000553591.1:c.129-5C= ENSP00000452421.1:n.129-5C=
ENST00000554056.5:n.123-5C=
ENST00000554065.1:c.-226-5C= ENSP00000451108.1:n.-226-5C=
ENST00000556293.5:n.131-5C=
ENST00000557229.5:n.131-5C=
NM_000270.3:c.12-5C= , LRG_91t1:c.12-5C= NP_000261.2:n.12-5C=
NM_000270.4:c.12-5C= MANE Select NP_000261.2:n.12-5C=