Canonical Allele Identifier: CA2687927944

Gene: PDP1

Linked Data

• gnomAD v4: 8-93923683-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923686dup , CM000670.2:g.93923686dup	GRCh38
NC_000008.10:g.94935914dup , CM000670.1:g.94935914dup	GRCh37
NC_000008.9:g.95005090dup	NCBI36
NG_012233.1:g.11753dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.*13dup MANE Select	ENSP00000297598.4:n.*13dup
ENST00000297598.4:c.*13dup	ENSP00000297598.4:n.*13dup
ENST00000396200.3:c.*13dup	ENSP00000379503.3:n.*13dup
ENST00000517764.1:c.*13dup	ENSP00000430380.1:n.*13dup
ENST00000520728.5:c.*13dup	ENSP00000428317.1:n.*13dup
NM_001161779.1:c.*13dup	NP_001155251.1:n.*13dup
NM_001161780.1:c.*13dup	NP_001155252.1:n.*13dup
NM_001161781.1:c.*13dup	NP_001155253.1:n.*13dup
NM_018444.3:c.*13dup	NP_060914.2:n.*13dup
XM_011517135.1:c.*13dup	XP_011515437.1:n.*13dup
XM_011517136.1:c.*13dup	XP_011515438.1:n.*13dup
XM_011517137.1:c.*13dup	XP_011515439.1:n.*13dup
XM_011517135.2:c.*13dup	XP_011515437.1:n.*13dup
XM_011517136.2:c.*13dup	XP_011515438.1:n.*13dup
XM_017013588.1:c.*13dup	XP_016869077.1:n.*13dup
NM_018444.4:c.*13dup MANE Select	NP_060914.2:n.*13dup
NM_001161780.2:c.*13dup	NP_001155252.1:n.*13dup
NM_001161781.2:c.*13dup	NP_001155253.1:n.*13dup
NM_001161779.2:c.*13dup	NP_001155251.1:n.*13dup