Canonical Allele Identifier: CA857071939
Gene: PDP1 HGNC NCBI

Linked Data

dbSNP Id: rs1419977863

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923460del , CM000670.2:g.93923460del GRCh38
NC_000008.10:g.94935688del , CM000670.1:g.94935688del GRCh37
NC_000008.9:g.95004864del NCBI36
NG_012233.1:g.11527del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1401del MANE Select ENSP00000297598.4:p.Met469CysfsTer?
ENST00000297598.4:c.1401del ENSP00000297598.4:p.Met469CysfsTer?
ENST00000396200.3:c.1476del ENSP00000379503.3:p.Met494CysfsTer?
ENST00000517764.1:c.1401del ENSP00000430380.1:p.Met469CysfsTer?
ENST00000520728.5:c.1401del ENSP00000428317.1:p.Met469CysfsTer?
NM_001161779.1:c.1476del NP_001155251.1:p.Met494CysfsTer?
NM_001161780.1:c.1476del NP_001155252.1:p.Met494CysfsTer?
NM_001161781.1:c.1401del NP_001155253.1:p.Met469CysfsTer?
NM_018444.3:c.1401del NP_060914.2:p.Met469CysfsTer?
XM_011517135.1:c.1455del XP_011515437.1:p.Met487CysfsTer?
XM_011517136.1:c.1401del XP_011515438.1:p.Met469CysfsTer?
XM_011517137.1:c.1401del XP_011515439.1:p.Met469CysfsTer?
XM_011517135.2:c.1455del XP_011515437.1:p.Met487CysfsTer?
XM_011517136.2:c.1401del XP_011515438.1:p.Met469CysfsTer?
XM_017013588.1:c.1563del XP_016869077.1:p.Met523CysfsTer?
NM_018444.4:c.1401del MANE Select NP_060914.2:p.Met469CysfsTer?
NM_001161780.2:c.1476del NP_001155252.1:p.Met494CysfsTer?
NM_001161781.2:c.1401del NP_001155253.1:p.Met469CysfsTer?
NM_001161779.2:c.1476del NP_001155251.1:p.Met494CysfsTer?