Canonical Allele Identifier: CA389145731

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943349G>T (hg19) ; chr14:g.20475190G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475190G>T , CM000676.2:g.20475190G>T	GRCh38
NC_000014.8:g.20943349G>T , CM000676.1:g.20943349G>T	GRCh37
NC_000014.7:g.20013189G>T	NCBI36
NG_009631.1:g.10808G>T , LRG_91:g.10808G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.707G>T	ENSP00000452421.2:p.Gly236Val
ENST00000556293.6:n.3013G>T
ENST00000556754.2:n.3956G>T
ENST00000557229.6:n.1019G>T
ENST00000697613.1:c.590G>T	ENSP00000513359.1:p.Gly197Val
ENST00000697614.1:c.353G>T	ENSP00000513360.1:p.Gly118Val
ENST00000697615.1:n.1418G>T
ENST00000361505.10:c.590G>T MANE Select	ENSP00000354532.6:p.Gly197Val
ENST00000361505.9:c.590G>T	ENSP00000354532.5:p.Gly197Val
ENST00000554056.5:n.898G>T
ENST00000556754.1:n.1807G>T
NM_000270.3:c.590G>T , LRG_91t1:c.590G>T	NP_000261.2:p.Gly197Val
NM_000270.4:c.590G>T MANE Select	NP_000261.2:p.Gly197Val