Canonical Allele Identifier: CA389144828

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20474470A>G , CM000676.2:g.20474470A>G	GRCh38
NC_000014.8:g.20942629A>G , CM000676.1:g.20942629A>G	GRCh37
NC_000014.7:g.20012469A>G	NCBI36
NG_009631.1:g.10088A>G , LRG_91:g.10088A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000270.4:c.182-2A>G MANE Select	NP_000261.2:n.182-2A>G
ENST00000361505.10:c.182-2A>G MANE Select	ENSP00000354532.6:n.182-2A>G
NM_000270.3:c.182-2A>G , LRG_91t1:c.182-2A>G	NP_000261.2:n.182-2A>G
ENST00000361505.9:c.182-2A>G	ENSP00000354532.5:n.182-2A>G
ENST00000553418.5:c.182-2A>G	ENSP00000450663.1:n.182-2A>G
ENST00000553591.1:c.299-2A>G	ENSP00000452421.1:n.299-2A>G
ENST00000553591.2:c.299-2A>G	ENSP00000452421.2:n.299-2A>G
ENST00000554056.5:n.293-2A>G
ENST00000554065.1:c.-56-2A>G	ENSP00000451108.1:n.-56-2A>G
ENST00000556293.6:n.2293A>G
ENST00000556754.1:n.1087A>G
ENST00000556754.2:n.3236A>G
ENST00000557229.5:n.301-2A>G
ENST00000557229.6:n.301-2A>G
ENST00000697613.1:c.182-2A>G	ENSP00000513359.1:n.182-2A>G
ENST00000697614.1:c.-56-2A>G	ENSP00000513360.1:n.-56-2A>G
ENST00000697615.1:n.700-2A>G