Canonical Allele Identifier: CA485161732

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940620C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472461C>T , CM000676.2:g.20472461C>T	GRCh38
NC_000014.8:g.20940620C>T , CM000676.1:g.20940620C>T	GRCh37
NC_000014.7:g.20010460C>T	NCBI36
NG_009631.1:g.8079C>T , LRG_91:g.8079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.282C>T	ENSP00000452421.2:p.Asn94=
ENST00000556293.6:n.284C>T
ENST00000556754.2:n.1227C>T
ENST00000557229.6:n.284C>T
ENST00000697613.1:c.165C>T	ENSP00000513359.1:p.Asn55=
ENST00000697614.1:c.-73C>T	ENSP00000513360.1:n.-73C>T
ENST00000697615.1:n.683C>T
ENST00000361505.10:c.165C>T MANE Select	ENSP00000354532.6:p.Asn55=
ENST00000361505.9:c.165C>T	ENSP00000354532.5:p.Asn55=
ENST00000553418.5:c.165C>T	ENSP00000450663.1:p.Asn55=
ENST00000553591.1:c.282C>T	ENSP00000452421.1:p.Asn94=
ENST00000554056.5:n.276C>T
ENST00000554065.1:c.-73C>T	ENSP00000451108.1:n.-73C>T
ENST00000556293.5:n.284C>T
ENST00000557229.5:n.284C>T
NM_000270.3:c.165C>T , LRG_91t1:c.165C>T	NP_000261.2:p.Asn55=
NM_000270.4:c.165C>T MANE Select	NP_000261.2:p.Asn55=