Canonical Allele Identifier: CA389144560

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940574A>T (hg19) ; chr14:g.20472415A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472415A>T , CM000676.2:g.20472415A>T	GRCh38
NC_000014.8:g.20940574A>T , CM000676.1:g.20940574A>T	GRCh37
NC_000014.7:g.20010414A>T	NCBI36
NG_009631.1:g.8033A>T , LRG_91:g.8033A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.236A>T	ENSP00000452421.2:p.Asp79Val
ENST00000556293.6:n.238A>T
ENST00000556754.2:n.1181A>T
ENST00000557229.6:n.238A>T
ENST00000697613.1:c.119A>T	ENSP00000513359.1:p.Asp40Val
ENST00000697614.1:c.-119A>T	ENSP00000513360.1:n.-119A>T
ENST00000697615.1:n.637A>T
ENST00000361505.10:c.119A>T MANE Select	ENSP00000354532.6:p.Asp40Val
ENST00000361505.9:c.119A>T	ENSP00000354532.5:p.Asp40Val
ENST00000553418.5:c.119A>T	ENSP00000450663.1:p.Asp40Val
ENST00000553591.1:c.236A>T	ENSP00000452421.1:p.Asp79Val
ENST00000554056.5:n.230A>T
ENST00000554065.1:c.-119A>T	ENSP00000451108.1:n.-119A>T
ENST00000556293.5:n.238A>T
ENST00000557229.5:n.238A>T
NM_000270.3:c.119A>T , LRG_91t1:c.119A>T	NP_000261.2:p.Asp40Val
NM_000270.4:c.119A>T MANE Select	NP_000261.2:p.Asp40Val