Canonical Allele Identifier: CA485162563

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20943239T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475080T>A , CM000676.2:g.20475080T>A	GRCh38
NC_000014.8:g.20943239T>A , CM000676.1:g.20943239T>A	GRCh37
NC_000014.7:g.20013079T>A	NCBI36
NG_009631.1:g.10698T>A , LRG_91:g.10698T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.597T>A	ENSP00000452421.2:p.Pro199=
ENST00000556293.6:n.2903T>A
ENST00000556754.2:n.3846T>A
ENST00000557229.6:n.909T>A
ENST00000697613.1:c.480T>A	ENSP00000513359.1:p.Pro160=
ENST00000697614.1:c.243T>A	ENSP00000513360.1:p.Pro81=
ENST00000697615.1:n.1308T>A
ENST00000361505.10:c.480T>A MANE Select	ENSP00000354532.6:p.Pro160=
ENST00000361505.9:c.480T>A	ENSP00000354532.5:p.Pro160=
ENST00000553591.1:c.597T>A	ENSP00000452421.1:p.Pro199=
ENST00000554056.5:n.788T>A
ENST00000556754.1:n.1697T>A
ENST00000557229.5:n.909T>A
NM_000270.3:c.480T>A , LRG_91t1:c.480T>A	NP_000261.2:p.Pro160=
NM_000270.4:c.480T>A MANE Select	NP_000261.2:p.Pro160=