Canonical Allele Identifier: CA389144807

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940631G>C (hg19) ; chr14:g.20472472G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472472G>C , CM000676.2:g.20472472G>C	GRCh38
NC_000014.8:g.20940631G>C , CM000676.1:g.20940631G>C	GRCh37
NC_000014.7:g.20010471G>C	NCBI36
NG_009631.1:g.8090G>C , LRG_91:g.8090G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.293G>C	ENSP00000452421.2:p.Ser98Thr
ENST00000556293.6:n.295G>C
ENST00000556754.2:n.1238G>C
ENST00000557229.6:n.295G>C
ENST00000697613.1:c.176G>C	ENSP00000513359.1:p.Ser59Thr
ENST00000697614.1:c.-62G>C	ENSP00000513360.1:n.-62G>C
ENST00000697615.1:n.694G>C
ENST00000361505.10:c.176G>C MANE Select	ENSP00000354532.6:p.Ser59Thr
ENST00000361505.9:c.176G>C	ENSP00000354532.5:p.Ser59Thr
ENST00000553418.5:c.176G>C	ENSP00000450663.1:p.Ser59Thr
ENST00000553591.1:c.293G>C	ENSP00000452421.1:p.Ser98Thr
ENST00000554056.5:n.287G>C
ENST00000554065.1:c.-62G>C	ENSP00000451108.1:n.-62G>C
ENST00000556293.5:n.295G>C
ENST00000557229.5:n.295G>C
NM_000270.3:c.176G>C , LRG_91t1:c.176G>C	NP_000261.2:p.Ser59Thr
NM_000270.4:c.176G>C MANE Select	NP_000261.2:p.Ser59Thr