Canonical Allele Identifier: CA7082232

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20476616G>A , CM000676.2:g.20476616G>A	GRCh38
NC_000014.8:g.20944775G>A , CM000676.1:g.20944775G>A	GRCh37
NC_000014.7:g.20014615G>A	NCBI36
NG_009631.1:g.12234G>A , LRG_91:g.12234G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000270.4:c.*15G>A MANE Select	NP_000261.2:n.*15G>A
ENST00000361505.10:c.*15G>A MANE Select	ENSP00000354532.6:n.*15G>A
NM_000270.3:c.*15G>A , LRG_91t1:c.*15G>A	NP_000261.2:n.*15G>A
ENST00000361505.9:c.*15G>A	ENSP00000354532.5:n.*15G>A
ENST00000553591.2:c.*15G>A	ENSP00000452421.2:n.*15G>A
ENST00000554056.5:n.1193G>A
ENST00000556293.6:n.3308G>A
ENST00000556754.1:n.2102G>A
ENST00000556754.2:n.4251G>A
ENST00000557229.6:n.1314G>A
ENST00000697613.1:c.*15G>A	ENSP00000513359.1:n.*15G>A
ENST00000697614.1:c.*15G>A	ENSP00000513360.1:n.*15G>A
ENST00000697615.1:n.1713G>A