Canonical Allele Identifier: CA389144091

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940489A>C (hg19) ; chr14:g.20472330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472330A>C , CM000676.2:g.20472330A>C	GRCh38
NC_000014.8:g.20940489A>C , CM000676.1:g.20940489A>C	GRCh37
NC_000014.7:g.20010329A>C	NCBI36
NG_009631.1:g.7948A>C , LRG_91:g.7948A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.151A>C	ENSP00000452421.2:p.Asn51His
ENST00000556293.6:n.153A>C
ENST00000556754.2:n.1096A>C
ENST00000557229.6:n.153A>C
ENST00000697613.1:c.34A>C	ENSP00000513359.1:p.Asn12His
ENST00000697614.1:c.-204A>C	ENSP00000513360.1:n.-204A>C
ENST00000697615.1:n.552A>C
ENST00000361505.10:c.34A>C MANE Select	ENSP00000354532.6:p.Asn12His
ENST00000361505.9:c.34A>C	ENSP00000354532.5:p.Asn12His
ENST00000553418.5:c.34A>C	ENSP00000450663.1:p.Asn12His
ENST00000553591.1:c.151A>C	ENSP00000452421.1:p.Asn51His
ENST00000554056.5:n.145A>C
ENST00000554065.1:c.-204A>C	ENSP00000451108.1:n.-204A>C
ENST00000556293.5:n.153A>C
ENST00000557229.5:n.153A>C
NM_000270.3:c.34A>C , LRG_91t1:c.34A>C	NP_000261.2:p.Asn12His
NM_000270.4:c.34A>C MANE Select	NP_000261.2:p.Asn12His