Canonical Allele Identifier: CA371696471

Gene: PDP1

Linked Data

• ClinVar Variation Id: 2122695
• ClinVar RCV Id: RCV003046996
• dbSNP Id: rs1586157708
• MyVariant Identifiers: chr8:g.94935570A>G (hg19) ; chr8:g.93923342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923342A>G , CM000670.2:g.93923342A>G	GRCh38
NC_000008.10:g.94935570A>G , CM000670.1:g.94935570A>G	GRCh37
NC_000008.9:g.95004746A>G	NCBI36
NG_012233.1:g.11409A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1283A>G MANE Select	ENSP00000297598.4:p.Asp428Gly
ENST00000297598.4:c.1283A>G	ENSP00000297598.4:p.Asp428Gly
ENST00000396200.3:c.1358A>G	ENSP00000379503.3:p.Asp453Gly
ENST00000517764.1:c.1283A>G	ENSP00000430380.1:p.Asp428Gly
ENST00000520728.5:c.1283A>G	ENSP00000428317.1:p.Asp428Gly
NM_001161779.1:c.1358A>G	NP_001155251.1:p.Asp453Gly
NM_001161780.1:c.1358A>G	NP_001155252.1:p.Asp453Gly
NM_001161781.1:c.1283A>G	NP_001155253.1:p.Asp428Gly
NM_018444.3:c.1283A>G	NP_060914.2:p.Asp428Gly
XM_011517135.1:c.1337A>G	XP_011515437.1:p.Asp446Gly
XM_011517136.1:c.1283A>G	XP_011515438.1:p.Asp428Gly
XM_011517137.1:c.1283A>G	XP_011515439.1:p.Asp428Gly
XM_011517135.2:c.1337A>G	XP_011515437.1:p.Asp446Gly
XM_011517136.2:c.1283A>G	XP_011515438.1:p.Asp428Gly
XM_017013588.1:c.1445A>G	XP_016869077.1:p.Asp482Gly
NM_018444.4:c.1283A>G MANE Select	NP_060914.2:p.Asp428Gly
NM_001161780.2:c.1358A>G	NP_001155252.1:p.Asp453Gly
NM_001161781.2:c.1283A>G	NP_001155253.1:p.Asp428Gly
NM_001161779.2:c.1358A>G	NP_001155251.1:p.Asp453Gly