Canonical Allele Identifier: CA389144085

Gene: PNP

Linked Data

• MyVariant Identifiers: chr14:g.20940488G>T (hg19) ; chr14:g.20472329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472329G>T , CM000676.2:g.20472329G>T	GRCh38
NC_000014.8:g.20940488G>T , CM000676.1:g.20940488G>T	GRCh37
NC_000014.7:g.20010328G>T	NCBI36
NG_009631.1:g.7947G>T , LRG_91:g.7947G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553591.2:c.150G>T	ENSP00000452421.2:p.Lys50Asn
ENST00000556293.6:n.152G>T
ENST00000556754.2:n.1095G>T
ENST00000557229.6:n.152G>T
ENST00000697613.1:c.33G>T	ENSP00000513359.1:p.Lys11Asn
ENST00000697614.1:c.-205G>T	ENSP00000513360.1:n.-205G>T
ENST00000697615.1:n.551G>T
ENST00000361505.10:c.33G>T MANE Select	ENSP00000354532.6:p.Lys11Asn
ENST00000361505.9:c.33G>T	ENSP00000354532.5:p.Lys11Asn
ENST00000553418.5:c.33G>T	ENSP00000450663.1:p.Lys11Asn
ENST00000553591.1:c.150G>T	ENSP00000452421.1:p.Lys50Asn
ENST00000554056.5:n.144G>T
ENST00000554065.1:c.-205G>T	ENSP00000451108.1:n.-205G>T
ENST00000556293.5:n.152G>T
ENST00000557229.5:n.152G>T
NM_000270.3:c.33G>T , LRG_91t1:c.33G>T	NP_000261.2:p.Lys11Asn
NM_000270.4:c.33G>T MANE Select	NP_000261.2:p.Lys11Asn