Canonical Allele Identifier: CA485161618

Gene: PNP

Linked Data

• gnomAD v4: 14-20472267-G-C
• MyVariant Identifiers: chr14:g.20940426G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472267G>C , CM000676.2:g.20472267G>C	GRCh38
NC_000014.8:g.20940426G>C , CM000676.1:g.20940426G>C	GRCh37
NC_000014.7:g.20010266G>C	NCBI36
NG_009631.1:g.7885G>C , LRG_91:g.7885G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.129-41G>C	ENSP00000452421.2:n.129-41G>C
ENST00000556293.6:n.131-41G>C
ENST00000556754.2:n.1033G>C
ENST00000557229.6:n.131-41G>C
ENST00000697613.1:c.12-41G>C	ENSP00000513359.1:n.12-41G>C
ENST00000697614.1:c.-226-41G>C	ENSP00000513360.1:n.-226-41G>C
ENST00000697615.1:n.489G>C
ENST00000361505.10:c.12-41G>C MANE Select	ENSP00000354532.6:n.12-41G>C
ENST00000361505.9:c.12-41G>C	ENSP00000354532.5:n.12-41G>C
ENST00000553418.5:c.12-41G>C	ENSP00000450663.1:n.12-41G>C
ENST00000553591.1:c.129-41G>C	ENSP00000452421.1:n.129-41G>C
ENST00000554056.5:n.123-41G>C
ENST00000554065.1:c.-226-41G>C	ENSP00000451108.1:n.-226-41G>C
ENST00000556293.5:n.131-41G>C
ENST00000557229.5:n.131-41G>C
NM_000270.3:c.12-41G>C , LRG_91t1:c.12-41G>C	NP_000261.2:n.12-41G>C
NM_000270.4:c.12-41G>C MANE Select	NP_000261.2:n.12-41G>C