Canonical Allele Identifier: CA2740962486
Gene: PDP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923565_93923566insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA , CM000670.2:g.93923565_93923566insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA GRCh38
NC_000008.10:g.94935793_94935794insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA , CM000670.1:g.94935793_94935794insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA GRCh37
NC_000008.9:g.95004969_95004970insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NCBI36
NG_012233.1:g.11632_11633insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA MANE Select ENSP00000297598.4:p.Met503GlyfsTer35
ENST00000297598.4:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA ENSP00000297598.4:p.Met503GlyfsTer35
ENST00000396200.3:c.1581_1582insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA ENSP00000379503.3:p.Met528GlyfsTer35
ENST00000517764.1:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA ENSP00000430380.1:p.Met503GlyfsTer35
ENST00000520728.5:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA ENSP00000428317.1:p.Met503GlyfsTer35
NM_001161779.1:c.1581_1582insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155251.1:p.Met528GlyfsTer35
NM_001161780.1:c.1581_1582insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155252.1:p.Met528GlyfsTer35
NM_001161781.1:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155253.1:p.Met503GlyfsTer35
NM_018444.3:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_060914.2:p.Met503GlyfsTer35
XM_011517135.1:c.1560_1561insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_011515437.1:p.Met521GlyfsTer35
XM_011517136.1:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_011515438.1:p.Met503GlyfsTer35
XM_011517137.1:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_011515439.1:p.Met503GlyfsTer35
XM_011517135.2:c.1560_1561insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_011515437.1:p.Met521GlyfsTer35
XM_011517136.2:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_011515438.1:p.Met503GlyfsTer35
XM_017013588.1:c.1668_1669insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA XP_016869077.1:p.Met557GlyfsTer35
NM_018444.4:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA MANE Select NP_060914.2:p.Met503GlyfsTer35
NM_001161780.2:c.1581_1582insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155252.1:p.Met528GlyfsTer35
NM_001161781.2:c.1506_1507insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155253.1:p.Met503GlyfsTer35
NM_001161779.2:c.1581_1582insGGAATGAAGTTCCTTGCCAGCAATGGAACAAAGCTGGATGGAGA NP_001155251.1:p.Met528GlyfsTer35