Canonical Allele Identifier: CA485162568

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943248T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475089T>A , CM000676.2:g.20475089T>A	GRCh38
NC_000014.8:g.20943248T>A , CM000676.1:g.20943248T>A	GRCh37
NC_000014.7:g.20013088T>A	NCBI36
NG_009631.1:g.10707T>A , LRG_91:g.10707T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.606T>A	ENSP00000452421.2:p.Ser202=
ENST00000556293.6:n.2912T>A
ENST00000556754.2:n.3855T>A
ENST00000557229.6:n.918T>A
ENST00000697613.1:c.489T>A	ENSP00000513359.1:p.Ser163=
ENST00000697614.1:c.252T>A	ENSP00000513360.1:p.Ser84=
ENST00000697615.1:n.1317T>A
ENST00000361505.10:c.489T>A MANE Select	ENSP00000354532.6:p.Ser163=
ENST00000361505.9:c.489T>A	ENSP00000354532.5:p.Ser163=
ENST00000553591.1:c.606T>A	ENSP00000452421.1:p.Ser202=
ENST00000554056.5:n.797T>A
ENST00000556754.1:n.1706T>A
ENST00000557229.5:n.918T>A
NM_000270.3:c.489T>A , LRG_91t1:c.489T>A	NP_000261.2:p.Ser163=
NM_000270.4:c.489T>A MANE Select	NP_000261.2:p.Ser163=