Canonical Allele Identifier: CA485161683

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940567C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472408C>T , CM000676.2:g.20472408C>T	GRCh38
NC_000014.8:g.20940567C>T , CM000676.1:g.20940567C>T	GRCh37
NC_000014.7:g.20010407C>T	NCBI36
NG_009631.1:g.8026C>T , LRG_91:g.8026C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.229C>T	ENSP00000452421.2:p.Leu77=
ENST00000556293.6:n.231C>T
ENST00000556754.2:n.1174C>T
ENST00000557229.6:n.231C>T
ENST00000697613.1:c.112C>T	ENSP00000513359.1:p.Leu38=
ENST00000697614.1:c.-126C>T	ENSP00000513360.1:n.-126C>T
ENST00000697615.1:n.630C>T
ENST00000361505.10:c.112C>T MANE Select	ENSP00000354532.6:p.Leu38=
ENST00000361505.9:c.112C>T	ENSP00000354532.5:p.Leu38=
ENST00000553418.5:c.112C>T	ENSP00000450663.1:p.Leu38=
ENST00000553591.1:c.229C>T	ENSP00000452421.1:p.Leu77=
ENST00000554056.5:n.223C>T
ENST00000554065.1:c.-126C>T	ENSP00000451108.1:n.-126C>T
ENST00000556293.5:n.231C>T
ENST00000557229.5:n.231C>T
NM_000270.3:c.112C>T , LRG_91t1:c.112C>T	NP_000261.2:p.Leu38=
NM_000270.4:c.112C>T MANE Select	NP_000261.2:p.Leu38=