Canonical Allele Identifier: CA371696444

Gene: PDP1

Linked Data

• ClinVar Variation Id: 2318297
• ClinVar RCV Id: RCV002910474
• dbSNP Id: rs1266586674
• gnomAD v2: 8-94935564-G-C
• gnomAD v3: 8-93923336-G-C
• gnomAD v4: 8-93923336-G-C
• MyVariant Identifiers: chr8:g.94935564G>C (hg19) ; chr8:g.93923336G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923336G>C , CM000670.2:g.93923336G>C	GRCh38
NC_000008.10:g.94935564G>C , CM000670.1:g.94935564G>C	GRCh37
NC_000008.9:g.95004740G>C	NCBI36
NG_012233.1:g.11403G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1277G>C MANE Select	ENSP00000297598.4:p.Arg426Thr
ENST00000297598.4:c.1277G>C	ENSP00000297598.4:p.Arg426Thr
ENST00000396200.3:c.1352G>C	ENSP00000379503.3:p.Arg451Thr
ENST00000517764.1:c.1277G>C	ENSP00000430380.1:p.Arg426Thr
ENST00000520728.5:c.1277G>C	ENSP00000428317.1:p.Arg426Thr
NM_001161779.1:c.1352G>C	NP_001155251.1:p.Arg451Thr
NM_001161780.1:c.1352G>C	NP_001155252.1:p.Arg451Thr
NM_001161781.1:c.1277G>C	NP_001155253.1:p.Arg426Thr
NM_018444.3:c.1277G>C	NP_060914.2:p.Arg426Thr
XM_011517135.1:c.1331G>C	XP_011515437.1:p.Arg444Thr
XM_011517136.1:c.1277G>C	XP_011515438.1:p.Arg426Thr
XM_011517137.1:c.1277G>C	XP_011515439.1:p.Arg426Thr
XM_011517135.2:c.1331G>C	XP_011515437.1:p.Arg444Thr
XM_011517136.2:c.1277G>C	XP_011515438.1:p.Arg426Thr
XM_017013588.1:c.1439G>C	XP_016869077.1:p.Arg480Thr
NM_018444.4:c.1277G>C MANE Select	NP_060914.2:p.Arg426Thr
NM_001161780.2:c.1352G>C	NP_001155252.1:p.Arg451Thr
NM_001161781.2:c.1277G>C	NP_001155253.1:p.Arg426Thr
NM_001161779.2:c.1352G>C	NP_001155251.1:p.Arg451Thr