Canonical Allele Identifier: CA4808762

Gene: PDP1

Linked Data

• dbSNP Id: rs780213686
• ExAC: 8:94935224 G / A
• gnomAD v2: 8-94935224-G-A
• gnomAD v3: 8-93922996-G-A
• gnomAD v4: 8-93922996-G-A
• MyVariant Identifiers: chr8:g.94935224G>A (hg19) ; chr8:g.93922996G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922996G>A , CM000670.2:g.93922996G>A	GRCh38
NC_000008.10:g.94935224G>A , CM000670.1:g.94935224G>A	GRCh37
NC_000008.9:g.95004400G>A	NCBI36
NG_012233.1:g.11063G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.937G>A MANE Select	ENSP00000297598.4:p.Asp313Asn
ENST00000297598.4:c.937G>A	ENSP00000297598.4:p.Asp313Asn
ENST00000396200.3:c.1012G>A	ENSP00000379503.3:p.Asp338Asn
ENST00000517764.1:c.937G>A	ENSP00000430380.1:p.Asp313Asn
ENST00000520728.5:c.937G>A	ENSP00000428317.1:p.Asp313Asn
NM_001161779.1:c.1012G>A	NP_001155251.1:p.Asp338Asn
NM_001161780.1:c.1012G>A	NP_001155252.1:p.Asp338Asn
NM_001161781.1:c.937G>A	NP_001155253.1:p.Asp313Asn
NM_018444.3:c.937G>A	NP_060914.2:p.Asp313Asn
XM_011517135.1:c.991G>A	XP_011515437.1:p.Asp331Asn
XM_011517136.1:c.937G>A	XP_011515438.1:p.Asp313Asn
XM_011517137.1:c.937G>A	XP_011515439.1:p.Asp313Asn
XM_011517135.2:c.991G>A	XP_011515437.1:p.Asp331Asn
XM_011517136.2:c.937G>A	XP_011515438.1:p.Asp313Asn
XM_017013588.1:c.1099G>A	XP_016869077.1:p.Asp367Asn
NM_018444.4:c.937G>A MANE Select	NP_060914.2:p.Asp313Asn
NM_001161780.2:c.1012G>A	NP_001155252.1:p.Asp338Asn
NM_001161781.2:c.937G>A	NP_001155253.1:p.Asp313Asn
NM_001161779.2:c.1012G>A	NP_001155251.1:p.Asp338Asn