Canonical Allele Identifier: CA257418183

Gene: PNP

Linked Data

• dbSNP Id: rs943480529
• MyVariant Identifiers: chr14:g.20943159T>C (hg19) ; chr14:g.20475000T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20475000T>C , CM000676.2:g.20475000T>C	GRCh38
NC_000014.8:g.20943159T>C , CM000676.1:g.20943159T>C	GRCh37
NC_000014.7:g.20012999T>C	NCBI36
NG_009631.1:g.10618T>C , LRG_91:g.10618T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.578+52T>C	ENSP00000452421.2:n.578+52T>C
ENST00000556293.6:n.2823T>C
ENST00000556754.2:n.3766T>C
ENST00000557229.6:n.829T>C
ENST00000697613.1:c.461+52T>C	ENSP00000513359.1:n.461+52T>C
ENST00000697614.1:c.224+52T>C	ENSP00000513360.1:n.224+52T>C
ENST00000697615.1:n.1228T>C
ENST00000361505.10:c.461+52T>C MANE Select	ENSP00000354532.6:n.461+52T>C
ENST00000361505.9:c.461+52T>C	ENSP00000354532.5:n.461+52T>C
ENST00000553591.1:c.578+52T>C	ENSP00000452421.1:n.578+52T>C
ENST00000554056.5:n.769+52T>C
ENST00000556754.1:n.1617T>C
ENST00000557229.5:n.829T>C
NM_000270.3:c.461+52T>C , LRG_91t1:c.461+52T>C	NP_000261.2:n.461+52T>C
NM_000270.4:c.461+52T>C MANE Select	NP_000261.2:n.461+52T>C