Canonical Allele Identifier: CA485450744

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943149A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20474990A>T , CM000676.2:g.20474990A>T	GRCh38
NC_000014.8:g.20943149A>T , CM000676.1:g.20943149A>T	GRCh37
NC_000014.7:g.20012989A>T	NCBI36
NG_009631.1:g.10608A>T , LRG_91:g.10608A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.578+42A>T	ENSP00000452421.2:n.578+42A>T
ENST00000556293.6:n.2813A>T
ENST00000556754.2:n.3756A>T
ENST00000557229.6:n.819A>T
ENST00000697613.1:c.461+42A>T	ENSP00000513359.1:n.461+42A>T
ENST00000697614.1:c.224+42A>T	ENSP00000513360.1:n.224+42A>T
ENST00000697615.1:n.1218A>T
ENST00000361505.10:c.461+42A>T MANE Select	ENSP00000354532.6:n.461+42A>T
ENST00000361505.9:c.461+42A>T	ENSP00000354532.5:n.461+42A>T
ENST00000553591.1:c.578+42A>T	ENSP00000452421.1:n.578+42A>T
ENST00000554056.5:n.769+42A>T
ENST00000556754.1:n.1607A>T
ENST00000557229.5:n.819A>T
NM_000270.3:c.461+42A>T , LRG_91t1:c.461+42A>T	NP_000261.2:n.461+42A>T
NM_000270.4:c.461+42A>T MANE Select	NP_000261.2:n.461+42A>T