Canonical Allele Identifier: CA4808752
Gene: PDP1 HGNC NCBI

Linked Data

dbSNP Id: rs772803719
gnomAD v2: 8-94935158-G-A
gnomAD v4: 8-93922930-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93922930G>A , CM000670.2:g.93922930G>A GRCh38
NC_000008.10:g.94935158G>A , CM000670.1:g.94935158G>A GRCh37
NC_000008.9:g.95004334G>A NCBI36
NG_012233.1:g.10997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.871G>A MANE Select ENSP00000297598.4:p.Asp291Asn
ENST00000297598.4:c.871G>A ENSP00000297598.4:p.Asp291Asn
ENST00000396200.3:c.946G>A ENSP00000379503.3:p.Asp316Asn
ENST00000517764.1:c.871G>A ENSP00000430380.1:p.Asp291Asn
ENST00000520728.5:c.871G>A ENSP00000428317.1:p.Asp291Asn
NM_001161779.1:c.946G>A NP_001155251.1:p.Asp316Asn
NM_001161780.1:c.946G>A NP_001155252.1:p.Asp316Asn
NM_001161781.1:c.871G>A NP_001155253.1:p.Asp291Asn
NM_018444.3:c.871G>A NP_060914.2:p.Asp291Asn
XM_011517135.1:c.925G>A XP_011515437.1:p.Asp309Asn
XM_011517136.1:c.871G>A XP_011515438.1:p.Asp291Asn
XM_011517137.1:c.871G>A XP_011515439.1:p.Asp291Asn
XM_011517135.2:c.925G>A XP_011515437.1:p.Asp309Asn
XM_011517136.2:c.871G>A XP_011515438.1:p.Asp291Asn
XM_017013588.1:c.1033G>A XP_016869077.1:p.Asp345Asn
NM_018444.4:c.871G>A MANE Select NP_060914.2:p.Asp291Asn
NM_001161780.2:c.946G>A NP_001155252.1:p.Asp316Asn
NM_001161781.2:c.871G>A NP_001155253.1:p.Asp291Asn
NM_001161779.2:c.946G>A NP_001155251.1:p.Asp316Asn