Canonical Allele Identifier: CA371696734

Gene: PDP1

Linked Data

• gnomAD v4: 8-93923404-G-C
• MyVariant Identifiers: chr8:g.94935632G>C (hg19) ; chr8:g.93923404G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923404G>C , CM000670.2:g.93923404G>C	GRCh38
NC_000008.10:g.94935632G>C , CM000670.1:g.94935632G>C	GRCh37
NC_000008.9:g.95004808G>C	NCBI36
NG_012233.1:g.11471G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1345G>C MANE Select	ENSP00000297598.4:p.Gly449Arg
ENST00000297598.4:c.1345G>C	ENSP00000297598.4:p.Gly449Arg
ENST00000396200.3:c.1420G>C	ENSP00000379503.3:p.Gly474Arg
ENST00000517764.1:c.1345G>C	ENSP00000430380.1:p.Gly449Arg
ENST00000520728.5:c.1345G>C	ENSP00000428317.1:p.Gly449Arg
NM_001161779.1:c.1420G>C	NP_001155251.1:p.Gly474Arg
NM_001161780.1:c.1420G>C	NP_001155252.1:p.Gly474Arg
NM_001161781.1:c.1345G>C	NP_001155253.1:p.Gly449Arg
NM_018444.3:c.1345G>C	NP_060914.2:p.Gly449Arg
XM_011517135.1:c.1399G>C	XP_011515437.1:p.Gly467Arg
XM_011517136.1:c.1345G>C	XP_011515438.1:p.Gly449Arg
XM_011517137.1:c.1345G>C	XP_011515439.1:p.Gly449Arg
XM_011517135.2:c.1399G>C	XP_011515437.1:p.Gly467Arg
XM_011517136.2:c.1345G>C	XP_011515438.1:p.Gly449Arg
XM_017013588.1:c.1507G>C	XP_016869077.1:p.Gly503Arg
NM_018444.4:c.1345G>C MANE Select	NP_060914.2:p.Gly449Arg
NM_001161780.2:c.1420G>C	NP_001155252.1:p.Gly474Arg
NM_001161781.2:c.1345G>C	NP_001155253.1:p.Gly449Arg
NM_001161779.2:c.1420G>C	NP_001155251.1:p.Gly474Arg