Canonical Allele Identifier: CA2687927879
Gene: PDP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923561_93923562del , CM000670.2:g.93923561_93923562del GRCh38
NC_000008.10:g.94935789_94935790del , CM000670.1:g.94935789_94935790del GRCh37
NC_000008.9:g.95004965_95004966del NCBI36
NG_012233.1:g.11628_11629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1502_1503del MANE Select ENSP00000297598.4:p.Ser501Ter
ENST00000297598.4:c.1502_1503del ENSP00000297598.4:p.Ser501Ter
ENST00000396200.3:c.1577_1578del ENSP00000379503.3:p.Ser526Ter
ENST00000517764.1:c.1502_1503del ENSP00000430380.1:p.Ser501Ter
ENST00000520728.5:c.1502_1503del ENSP00000428317.1:p.Ser501Ter
NM_001161779.1:c.1577_1578del NP_001155251.1:p.Ser526Ter
NM_001161780.1:c.1577_1578del NP_001155252.1:p.Ser526Ter
NM_001161781.1:c.1502_1503del NP_001155253.1:p.Ser501Ter
NM_018444.3:c.1502_1503del NP_060914.2:p.Ser501Ter
XM_011517135.1:c.1556_1557del XP_011515437.1:p.Ser519Ter
XM_011517136.1:c.1502_1503del XP_011515438.1:p.Ser501Ter
XM_011517137.1:c.1502_1503del XP_011515439.1:p.Ser501Ter
XM_011517135.2:c.1556_1557del XP_011515437.1:p.Ser519Ter
XM_011517136.2:c.1502_1503del XP_011515438.1:p.Ser501Ter
XM_017013588.1:c.1664_1665del XP_016869077.1:p.Ser555Ter
NM_018444.4:c.1502_1503del MANE Select NP_060914.2:p.Ser501Ter
NM_001161780.2:c.1577_1578del NP_001155252.1:p.Ser526Ter
NM_001161781.2:c.1502_1503del NP_001155253.1:p.Ser501Ter
NM_001161779.2:c.1577_1578del NP_001155251.1:p.Ser526Ter