Canonical Allele Identifier: CA1803280896
Gene: PDP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923291A= , CM000670.2:g.93923291A= GRCh38
NC_000008.10:g.94935519A= , CM000670.1:g.94935519A= GRCh37
NC_000008.9:g.95004695A= NCBI36
NG_012233.1:g.11358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1232A= MANE Select ENSP00000297598.4:p.Lys411=
ENST00000297598.4:c.1232A= ENSP00000297598.4:p.Lys411=
ENST00000396200.3:c.1307A= ENSP00000379503.3:p.Lys436=
ENST00000517764.1:c.1232A= ENSP00000430380.1:p.Lys411=
ENST00000520728.5:c.1232A= ENSP00000428317.1:p.Lys411=
NM_001161779.1:c.1307A= NP_001155251.1:p.Lys436=
NM_001161780.1:c.1307A= NP_001155252.1:p.Lys436=
NM_001161781.1:c.1232A= NP_001155253.1:p.Lys411=
NM_018444.3:c.1232A= NP_060914.2:p.Lys411=
XM_011517135.1:c.1286A= XP_011515437.1:p.Lys429=
XM_011517136.1:c.1232A= XP_011515438.1:p.Lys411=
XM_011517137.1:c.1232A= XP_011515439.1:p.Lys411=
XM_011517135.2:c.1286A= XP_011515437.1:p.Lys429=
XM_011517136.2:c.1232A= XP_011515438.1:p.Lys411=
XM_017013588.1:c.1394A= XP_016869077.1:p.Lys465=
NM_018444.4:c.1232A= MANE Select NP_060914.2:p.Lys411=
NM_001161780.2:c.1307A= NP_001155252.1:p.Lys436=
NM_001161781.2:c.1232A= NP_001155253.1:p.Lys411=
NM_001161779.2:c.1307A= NP_001155251.1:p.Lys436=