Canonical Allele Identifier: CA2122043860

Gene: PNP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20472300_20472301delinsTC , CM000676.2:g.20472300_20472301delinsTC	GRCh38
NC_000014.8:g.20940459_20940460delinsTC , CM000676.1:g.20940459_20940460delinsTC	GRCh37
NC_000014.7:g.20010299_20010300delinsTC	NCBI36
NG_009631.1:g.7918_7919delinsTC , LRG_91:g.7918_7919delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000553591.2:c.129-8_129-7delinsTC	ENSP00000452421.2:n.129-8_129-7delinsTC
ENST00000556293.6:n.131-8_131-7delinsTC
ENST00000556754.2:n.1066_1067delinsTC
ENST00000557229.6:n.131-8_131-7delinsTC
ENST00000697613.1:c.12-8_12-7delinsTC	ENSP00000513359.1:n.12-8_12-7delinsTC
ENST00000697614.1:c.-226-8_-226-7delinsTC	ENSP00000513360.1:n.-226-8_-226-7delinsTC...
ENST00000697615.1:n.522_523delinsTC
ENST00000361505.10:c.12-8_12-7delinsTC MANE Select	ENSP00000354532.6:n.12-8_12-7delinsTC
ENST00000361505.9:c.12-8_12-7delinsTC	ENSP00000354532.5:n.12-8_12-7delinsTC
ENST00000553418.5:c.12-8_12-7delinsTC	ENSP00000450663.1:n.12-8_12-7delinsTC
ENST00000553591.1:c.129-8_129-7delinsTC	ENSP00000452421.1:n.129-8_129-7delinsTC
ENST00000554056.5:n.123-8_123-7delinsTC
ENST00000554065.1:c.-226-8_-226-7delinsTC	ENSP00000451108.1:n.-226-8_-226-7delinsTC...
ENST00000556293.5:n.131-8_131-7delinsTC
ENST00000557229.5:n.131-8_131-7delinsTC
NM_000270.3:c.12-8_12-7delinsTC , LRG_91t1:c.12-8_12-7delinsTC	NP_000261.2:n.12-8_12-7delinsTC
NM_000270.4:c.12-8_12-7delinsTC MANE Select	NP_000261.2:n.12-8_12-7delinsTC