Canonical Allele Identifier: CA485162573

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943254C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475095C>A , CM000676.2:g.20475095C>A	GRCh38
NC_000014.8:g.20943254C>A , CM000676.1:g.20943254C>A	GRCh37
NC_000014.7:g.20013094C>A	NCBI36
NG_009631.1:g.10713C>A , LRG_91:g.10713C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.612C>A	ENSP00000452421.2:p.Ala204=
ENST00000556293.6:n.2918C>A
ENST00000556754.2:n.3861C>A
ENST00000557229.6:n.924C>A
ENST00000697613.1:c.495C>A	ENSP00000513359.1:p.Ala165=
ENST00000697614.1:c.258C>A	ENSP00000513360.1:p.Ala86=
ENST00000697615.1:n.1323C>A
ENST00000361505.10:c.495C>A MANE Select	ENSP00000354532.6:p.Ala165=
ENST00000361505.9:c.495C>A	ENSP00000354532.5:p.Ala165=
ENST00000553591.1:c.612C>A	ENSP00000452421.1:p.Ala204=
ENST00000554056.5:n.803C>A
ENST00000556754.1:n.1712C>A
ENST00000557229.5:n.924C>A
NM_000270.3:c.495C>A , LRG_91t1:c.495C>A	NP_000261.2:p.Ala165=
NM_000270.4:c.495C>A MANE Select	NP_000261.2:p.Ala165=