Canonical Allele Identifier: CA371697482
Gene: PDP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923518G>A , CM000670.2:g.93923518G>A GRCh38
NC_000008.10:g.94935746G>A , CM000670.1:g.94935746G>A GRCh37
NC_000008.9:g.95004922G>A NCBI36
NG_012233.1:g.11585G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1459G>A MANE Select ENSP00000297598.4:p.Val487Met
ENST00000297598.4:c.1459G>A ENSP00000297598.4:p.Val487Met
ENST00000396200.3:c.1534G>A ENSP00000379503.3:p.Val512Met
ENST00000517764.1:c.1459G>A ENSP00000430380.1:p.Val487Met
ENST00000520728.5:c.1459G>A ENSP00000428317.1:p.Val487Met
NM_001161779.1:c.1534G>A NP_001155251.1:p.Val512Met
NM_001161780.1:c.1534G>A NP_001155252.1:p.Val512Met
NM_001161781.1:c.1459G>A NP_001155253.1:p.Val487Met
NM_018444.3:c.1459G>A NP_060914.2:p.Val487Met
XM_011517135.1:c.1513G>A XP_011515437.1:p.Val505Met
XM_011517136.1:c.1459G>A XP_011515438.1:p.Val487Met
XM_011517137.1:c.1459G>A XP_011515439.1:p.Val487Met
XM_011517135.2:c.1513G>A XP_011515437.1:p.Val505Met
XM_011517136.2:c.1459G>A XP_011515438.1:p.Val487Met
XM_017013588.1:c.1621G>A XP_016869077.1:p.Val541Met
NM_018444.4:c.1459G>A MANE Select NP_060914.2:p.Val487Met
NM_001161780.2:c.1534G>A NP_001155252.1:p.Val512Met
NM_001161781.2:c.1459G>A NP_001155253.1:p.Val487Met
NM_001161779.2:c.1534G>A NP_001155251.1:p.Val512Met