Canonical Allele Identifier: CA2575472436

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472266G>A , CM000676.2:g.20472266G>A	GRCh38
NC_000014.8:g.20940425G>A , CM000676.1:g.20940425G>A	GRCh37
NC_000014.7:g.20010265G>A	NCBI36
NG_009631.1:g.7884G>A , LRG_91:g.7884G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.129-42G>A	ENSP00000452421.2:n.129-42G>A
ENST00000556293.6:n.131-42G>A
ENST00000556754.2:n.1032G>A
ENST00000557229.6:n.131-42G>A
ENST00000697613.1:c.12-42G>A	ENSP00000513359.1:n.12-42G>A
ENST00000697614.1:c.-226-42G>A	ENSP00000513360.1:n.-226-42G>A
ENST00000697615.1:n.488G>A
ENST00000361505.10:c.12-42G>A MANE Select	ENSP00000354532.6:n.12-42G>A
ENST00000361505.9:c.12-42G>A	ENSP00000354532.5:n.12-42G>A
ENST00000553418.5:c.12-42G>A	ENSP00000450663.1:n.12-42G>A
ENST00000553591.1:c.129-42G>A	ENSP00000452421.1:n.129-42G>A
ENST00000554056.5:n.123-42G>A
ENST00000554065.1:c.-226-42G>A	ENSP00000451108.1:n.-226-42G>A
ENST00000556293.5:n.131-42G>A
ENST00000557229.5:n.131-42G>A
NM_000270.3:c.12-42G>A , LRG_91t1:c.12-42G>A	NP_000261.2:n.12-42G>A
NM_000270.4:c.12-42G>A MANE Select	NP_000261.2:n.12-42G>A