Canonical Allele Identifier: CA2575472438

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472298T>C , CM000676.2:g.20472298T>C	GRCh38
NC_000014.8:g.20940457T>C , CM000676.1:g.20940457T>C	GRCh37
NC_000014.7:g.20010297T>C	NCBI36
NG_009631.1:g.7916T>C , LRG_91:g.7916T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.129-10T>C	ENSP00000452421.2:n.129-10T>C
ENST00000556293.6:n.131-10T>C
ENST00000556754.2:n.1064T>C
ENST00000557229.6:n.131-10T>C
ENST00000697613.1:c.12-10T>C	ENSP00000513359.1:n.12-10T>C
ENST00000697614.1:c.-226-10T>C	ENSP00000513360.1:n.-226-10T>C
ENST00000697615.1:n.520T>C
ENST00000361505.10:c.12-10T>C MANE Select	ENSP00000354532.6:n.12-10T>C
ENST00000361505.9:c.12-10T>C	ENSP00000354532.5:n.12-10T>C
ENST00000553418.5:c.12-10T>C	ENSP00000450663.1:n.12-10T>C
ENST00000553591.1:c.129-10T>C	ENSP00000452421.1:n.129-10T>C
ENST00000554056.5:n.123-10T>C
ENST00000554065.1:c.-226-10T>C	ENSP00000451108.1:n.-226-10T>C
ENST00000556293.5:n.131-10T>C
ENST00000557229.5:n.131-10T>C
NM_000270.3:c.12-10T>C , LRG_91t1:c.12-10T>C	NP_000261.2:n.12-10T>C
NM_000270.4:c.12-10T>C MANE Select	NP_000261.2:n.12-10T>C