Canonical Allele Identifier: CA485162671

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943350C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475191C>T , CM000676.2:g.20475191C>T	GRCh38
NC_000014.8:g.20943350C>T , CM000676.1:g.20943350C>T	GRCh37
NC_000014.7:g.20013190C>T	NCBI36
NG_009631.1:g.10809C>T , LRG_91:g.10809C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.708C>T	ENSP00000452421.2:p.Gly236=
ENST00000556293.6:n.3014C>T
ENST00000556754.2:n.3957C>T
ENST00000557229.6:n.1020C>T
ENST00000697613.1:c.591C>T	ENSP00000513359.1:p.Gly197=
ENST00000697614.1:c.354C>T	ENSP00000513360.1:p.Gly118=
ENST00000697615.1:n.1419C>T
ENST00000361505.10:c.591C>T MANE Select	ENSP00000354532.6:p.Gly197=
ENST00000361505.9:c.591C>T	ENSP00000354532.5:p.Gly197=
ENST00000554056.5:n.899C>T
ENST00000556754.1:n.1808C>T
NM_000270.3:c.591C>T , LRG_91t1:c.591C>T	NP_000261.2:p.Gly197=
NM_000270.4:c.591C>T MANE Select	NP_000261.2:p.Gly197=