Canonical Allele Identifier: CA485161738

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940626C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472467C>G , CM000676.2:g.20472467C>G	GRCh38
NC_000014.8:g.20940626C>G , CM000676.1:g.20940626C>G	GRCh37
NC_000014.7:g.20010466C>G	NCBI36
NG_009631.1:g.8085C>G , LRG_91:g.8085C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.288C>G	ENSP00000452421.2:p.Pro96=
ENST00000556293.6:n.290C>G
ENST00000556754.2:n.1233C>G
ENST00000557229.6:n.290C>G
ENST00000697613.1:c.171C>G	ENSP00000513359.1:p.Pro57=
ENST00000697614.1:c.-67C>G	ENSP00000513360.1:n.-67C>G
ENST00000697615.1:n.689C>G
ENST00000361505.10:c.171C>G MANE Select	ENSP00000354532.6:p.Pro57=
ENST00000361505.9:c.171C>G	ENSP00000354532.5:p.Pro57=
ENST00000553418.5:c.171C>G	ENSP00000450663.1:p.Pro57=
ENST00000553591.1:c.288C>G	ENSP00000452421.1:p.Pro96=
ENST00000554056.5:n.282C>G
ENST00000554065.1:c.-67C>G	ENSP00000451108.1:n.-67C>G
ENST00000556293.5:n.290C>G
ENST00000557229.5:n.290C>G
NM_000270.3:c.171C>G , LRG_91t1:c.171C>G	NP_000261.2:p.Pro57=
NM_000270.4:c.171C>G MANE Select	NP_000261.2:p.Pro57=