Canonical Allele Identifier: CA16605443
Gene: PDP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391847
ClinVar RCV Id: RCV000425732
dbSNP Id: rs1057524261
MyVariant Identifiers: chr8:g.94935550G>A (hg19) chr8:g.93923322G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923322G>A , CM000670.2:g.93923322G>A GRCh38
NC_000008.10:g.94935550G>A , CM000670.1:g.94935550G>A GRCh37
NC_000008.9:g.95004726G>A NCBI36
NG_012233.1:g.11389G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297598.5:c.1263G>A MANE Select ENSP00000297598.4:p.Trp421Ter
ENST00000297598.4:c.1263G>A ENSP00000297598.4:p.Trp421Ter
ENST00000396200.3:c.1338G>A ENSP00000379503.3:p.Trp446Ter
ENST00000517764.1:c.1263G>A ENSP00000430380.1:p.Trp421Ter
ENST00000520728.5:c.1263G>A ENSP00000428317.1:p.Trp421Ter
NM_001161779.1:c.1338G>A NP_001155251.1:p.Trp446Ter
NM_001161780.1:c.1338G>A NP_001155252.1:p.Trp446Ter
NM_001161781.1:c.1263G>A NP_001155253.1:p.Trp421Ter
NM_018444.3:c.1263G>A NP_060914.2:p.Trp421Ter
XM_011517135.1:c.1317G>A XP_011515437.1:p.Trp439Ter
XM_011517136.1:c.1263G>A XP_011515438.1:p.Trp421Ter
XM_011517137.1:c.1263G>A XP_011515439.1:p.Trp421Ter
XM_011517135.2:c.1317G>A XP_011515437.1:p.Trp439Ter
XM_011517136.2:c.1263G>A XP_011515438.1:p.Trp421Ter
XM_017013588.1:c.1425G>A XP_016869077.1:p.Trp475Ter
NM_018444.4:c.1263G>A MANE Select NP_060914.2:p.Trp421Ter
NM_001161780.2:c.1338G>A NP_001155252.1:p.Trp446Ter
NM_001161781.2:c.1263G>A NP_001155253.1:p.Trp421Ter
NM_001161779.2:c.1338G>A NP_001155251.1:p.Trp446Ter
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