Canonical Allele Identifier: CA2687927973

Gene: PDP1

Linked Data

• gnomAD v4: 8-93923701-A-ATGTTGTAGGGGCGTATCAAAACCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923701_93923702insTGTTGTAGGGGCGTATCAAAACCAAG , CM000670.2:g.93923701_93923702insTGTTGTAGGGGCGTATCAAAACCAAG	GRCh38
NC_000008.10:g.94935929_94935930insTGTTGTAGGGGCGTATCAAAACCAAG , CM000670.1:g.94935929_94935930insTGTTGTAGGGGCGTATCAAAACCAAG	GRCh37
NC_000008.9:g.95005105_95005106insTGTTGTAGGGGCGTATCAAAACCAAG	NCBI36
NG_012233.1:g.11768_11769insTGTTGTAGGGGCGTATCAAAACCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG MANE Select	ENSP00000297598.4:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
ENST00000297598.4:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	ENSP00000297598.4:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
ENST00000396200.3:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	ENSP00000379503.3:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
ENST00000517764.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	ENSP00000430380.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
ENST00000520728.5:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	ENSP00000428317.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161779.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155251.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161780.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155252.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161781.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155253.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_018444.3:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_060914.2:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_011517135.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_011515437.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_011517136.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_011515438.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_011517137.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_011515439.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_011517135.2:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_011515437.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_011517136.2:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_011515438.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
XM_017013588.1:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	XP_016869077.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_018444.4:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG MANE Select	NP_060914.2:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161780.2:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155252.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161781.2:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155253.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG
NM_001161779.2:c.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG	NP_001155251.1:n.*28_*29insTGTTGTAGGGGCGTATCAAAACCAAG