Canonical Allele Identifier: CA485161898

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940635A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472476A>C , CM000676.2:g.20472476A>C	GRCh38
NC_000014.8:g.20940635A>C , CM000676.1:g.20940635A>C	GRCh37
NC_000014.7:g.20010475A>C	NCBI36
NG_009631.1:g.8094A>C , LRG_91:g.8094A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.297A>C	ENSP00000452421.2:p.Thr99=
ENST00000556293.6:n.299A>C
ENST00000556754.2:n.1242A>C
ENST00000557229.6:n.299A>C
ENST00000697613.1:c.180A>C	ENSP00000513359.1:p.Thr60=
ENST00000697614.1:c.-58A>C	ENSP00000513360.1:n.-58A>C
ENST00000697615.1:n.698A>C
ENST00000361505.10:c.180A>C MANE Select	ENSP00000354532.6:p.Thr60=
ENST00000361505.9:c.180A>C	ENSP00000354532.5:p.Thr60=
ENST00000553418.5:c.180A>C	ENSP00000450663.1:p.Thr60=
ENST00000553591.1:c.297A>C	ENSP00000452421.1:p.Thr99=
ENST00000554056.5:n.291A>C
ENST00000554065.1:c.-58A>C	ENSP00000451108.1:n.-58A>C
ENST00000556293.5:n.299A>C
ENST00000557229.5:n.299A>C
NM_000270.3:c.180A>C , LRG_91t1:c.180A>C	NP_000261.2:p.Thr60=
NM_000270.4:c.180A>C MANE Select	NP_000261.2:p.Thr60=