Canonical Allele Identifier: CA389144286

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940522C>G (hg19) ; chr14:g.20472363C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472363C>G , CM000676.2:g.20472363C>G	GRCh38
NC_000014.8:g.20940522C>G , CM000676.1:g.20940522C>G	GRCh37
NC_000014.7:g.20010362C>G	NCBI36
NG_009631.1:g.7981C>G , LRG_91:g.7981C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.184C>G	ENSP00000452421.2:p.His62Asp
ENST00000556293.6:n.186C>G
ENST00000556754.2:n.1129C>G
ENST00000557229.6:n.186C>G
ENST00000697613.1:c.67C>G	ENSP00000513359.1:p.His23Asp
ENST00000697614.1:c.-171C>G	ENSP00000513360.1:n.-171C>G
ENST00000697615.1:n.585C>G
ENST00000361505.10:c.67C>G MANE Select	ENSP00000354532.6:p.His23Asp
ENST00000361505.9:c.67C>G	ENSP00000354532.5:p.His23Asp
ENST00000553418.5:c.67C>G	ENSP00000450663.1:p.His23Asp
ENST00000553591.1:c.184C>G	ENSP00000452421.1:p.His62Asp
ENST00000554056.5:n.178C>G
ENST00000554065.1:c.-171C>G	ENSP00000451108.1:n.-171C>G
ENST00000556293.5:n.186C>G
ENST00000557229.5:n.186C>G
NM_000270.3:c.67C>G , LRG_91t1:c.67C>G	NP_000261.2:p.His23Asp
NM_000270.4:c.67C>G MANE Select	NP_000261.2:p.His23Asp