Canonical Allele Identifier: CA2122045110

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475090G= , CM000676.2:g.20475090G=	GRCh38
NC_000014.8:g.20943249G= , CM000676.1:g.20943249G=	GRCh37
NC_000014.7:g.20013089G=	NCBI36
NG_009631.1:g.10708G= , LRG_91:g.10708G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.607G=	ENSP00000452421.2:p.Asp203=
ENST00000556293.6:n.2913G=
ENST00000556754.2:n.3856G=
ENST00000557229.6:n.919G=
ENST00000697613.1:c.490G=	ENSP00000513359.1:p.Asp164=
ENST00000697614.1:c.253G=	ENSP00000513360.1:p.Asp85=
ENST00000697615.1:n.1318G=
ENST00000361505.10:c.490G= MANE Select	ENSP00000354532.6:p.Asp164=
ENST00000361505.9:c.490G=	ENSP00000354532.5:p.Asp164=
ENST00000553591.1:c.607G=	ENSP00000452421.1:p.Asp203=
ENST00000554056.5:n.798G=
ENST00000556754.1:n.1707G=
ENST00000557229.5:n.919G=
NM_000270.3:c.490G= , LRG_91t1:c.490G=	NP_000261.2:p.Asp164=
NM_000270.4:c.490G= MANE Select	NP_000261.2:p.Asp164=