Canonical Allele Identifier: CA1803280781

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922908_93922911delinsCCTT , CM000670.2:g.93922908_93922911delinsCCTT	GRCh38
NC_000008.10:g.94935136_94935139delinsCCTT , CM000670.1:g.94935136_94935139delinsCCTT	GRCh37
NC_000008.9:g.95004312_95004315delinsCCTT	NCBI36
NG_012233.1:g.10975_10978delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.849_852delinsCCTT MANE Select	ENSP00000297598.4:p.Asp283=
ENST00000297598.4:c.849_852delinsCCTT	ENSP00000297598.4:p.Asp283=
ENST00000396200.3:c.924_927delinsCCTT	ENSP00000379503.3:p.Asp308=
ENST00000517764.1:c.849_852delinsCCTT	ENSP00000430380.1:p.Asp283=
ENST00000520728.5:c.849_852delinsCCTT	ENSP00000428317.1:p.Asp283=
NM_001161779.1:c.924_927delinsCCTT	NP_001155251.1:p.Asp308=
NM_001161780.1:c.924_927delinsCCTT	NP_001155252.1:p.Asp308=
NM_001161781.1:c.849_852delinsCCTT	NP_001155253.1:p.Asp283=
NM_018444.3:c.849_852delinsCCTT	NP_060914.2:p.Asp283=
XM_011517135.1:c.903_906delinsCCTT	XP_011515437.1:p.Asp301=
XM_011517136.1:c.849_852delinsCCTT	XP_011515438.1:p.Asp283=
XM_011517137.1:c.849_852delinsCCTT	XP_011515439.1:p.Asp283=
XM_011517135.2:c.903_906delinsCCTT	XP_011515437.1:p.Asp301=
XM_011517136.2:c.849_852delinsCCTT	XP_011515438.1:p.Asp283=
XM_017013588.1:c.1011_1014delinsCCTT	XP_016869077.1:p.Asp337=
NM_018444.4:c.849_852delinsCCTT MANE Select	NP_060914.2:p.Asp283=
NM_001161780.2:c.924_927delinsCCTT	NP_001155252.1:p.Asp308=
NM_001161781.2:c.849_852delinsCCTT	NP_001155253.1:p.Asp283=
NM_001161779.2:c.924_927delinsCCTT	NP_001155251.1:p.Asp308=