Canonical Allele Identifier: CA371694551
Gene: PDP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93922939G>T , CM000670.2:g.93922939G>T GRCh38
NC_000008.10:g.94935167G>T , CM000670.1:g.94935167G>T GRCh37
NC_000008.9:g.95004343G>T NCBI36
NG_012233.1:g.11006G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.880G>T MANE Select ENSP00000297598.4:p.Ala294Ser
ENST00000297598.4:c.880G>T ENSP00000297598.4:p.Ala294Ser
ENST00000396200.3:c.955G>T ENSP00000379503.3:p.Ala319Ser
ENST00000517764.1:c.880G>T ENSP00000430380.1:p.Ala294Ser
ENST00000520728.5:c.880G>T ENSP00000428317.1:p.Ala294Ser
NM_001161779.1:c.955G>T NP_001155251.1:p.Ala319Ser
NM_001161780.1:c.955G>T NP_001155252.1:p.Ala319Ser
NM_001161781.1:c.880G>T NP_001155253.1:p.Ala294Ser
NM_018444.3:c.880G>T NP_060914.2:p.Ala294Ser
XM_011517135.1:c.934G>T XP_011515437.1:p.Ala312Ser
XM_011517136.1:c.880G>T XP_011515438.1:p.Ala294Ser
XM_011517137.1:c.880G>T XP_011515439.1:p.Ala294Ser
XM_011517135.2:c.934G>T XP_011515437.1:p.Ala312Ser
XM_011517136.2:c.880G>T XP_011515438.1:p.Ala294Ser
XM_017013588.1:c.1042G>T XP_016869077.1:p.Ala348Ser
NM_018444.4:c.880G>T MANE Select NP_060914.2:p.Ala294Ser
NM_001161780.2:c.955G>T NP_001155252.1:p.Ala319Ser
NM_001161781.2:c.880G>T NP_001155253.1:p.Ala294Ser
NM_001161779.2:c.955G>T NP_001155251.1:p.Ala319Ser