Canonical Allele Identifier: CA485161627

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940494T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472335T>A , CM000676.2:g.20472335T>A	GRCh38
NC_000014.8:g.20940494T>A , CM000676.1:g.20940494T>A	GRCh37
NC_000014.7:g.20010334T>A	NCBI36
NG_009631.1:g.7953T>A , LRG_91:g.7953T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.156T>A	ENSP00000452421.2:p.Thr52=
ENST00000556293.6:n.158T>A
ENST00000556754.2:n.1101T>A
ENST00000557229.6:n.158T>A
ENST00000697613.1:c.39T>A	ENSP00000513359.1:p.Thr13=
ENST00000697614.1:c.-199T>A	ENSP00000513360.1:n.-199T>A
ENST00000697615.1:n.557T>A
ENST00000361505.10:c.39T>A MANE Select	ENSP00000354532.6:p.Thr13=
ENST00000361505.9:c.39T>A	ENSP00000354532.5:p.Thr13=
ENST00000553418.5:c.39T>A	ENSP00000450663.1:p.Thr13=
ENST00000553591.1:c.156T>A	ENSP00000452421.1:p.Thr52=
ENST00000554056.5:n.150T>A
ENST00000554065.1:c.-199T>A	ENSP00000451108.1:n.-199T>A
ENST00000556293.5:n.158T>A
ENST00000557229.5:n.158T>A
NM_000270.3:c.39T>A , LRG_91t1:c.39T>A	NP_000261.2:p.Thr13=
NM_000270.4:c.39T>A MANE Select	NP_000261.2:p.Thr13=