Canonical Allele Identifier: CA1803280773

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922898_93922904delinsATGGTGT , CM000670.2:g.93922898_93922904delinsATGGTGT	GRCh38
NC_000008.10:g.94935126_94935132delinsATGGTGT , CM000670.1:g.94935126_94935132delinsATGGTGT	GRCh37
NC_000008.9:g.95004302_95004308delinsATGGTGT	NCBI36
NG_012233.1:g.10965_10971delinsATGGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.839_845delinsATGGTGT MANE Select	ENSP00000297598.4:p.Asp280=
ENST00000297598.4:c.839_845delinsATGGTGT	ENSP00000297598.4:p.Asp280=
ENST00000396200.3:c.914_920delinsATGGTGT	ENSP00000379503.3:p.Asp305=
ENST00000517764.1:c.839_845delinsATGGTGT	ENSP00000430380.1:p.Asp280=
ENST00000520728.5:c.839_845delinsATGGTGT	ENSP00000428317.1:p.Asp280=
NM_001161779.1:c.914_920delinsATGGTGT	NP_001155251.1:p.Asp305=
NM_001161780.1:c.914_920delinsATGGTGT	NP_001155252.1:p.Asp305=
NM_001161781.1:c.839_845delinsATGGTGT	NP_001155253.1:p.Asp280=
NM_018444.3:c.839_845delinsATGGTGT	NP_060914.2:p.Asp280=
XM_011517135.1:c.893_899delinsATGGTGT	XP_011515437.1:p.Asp298=
XM_011517136.1:c.839_845delinsATGGTGT	XP_011515438.1:p.Asp280=
XM_011517137.1:c.839_845delinsATGGTGT	XP_011515439.1:p.Asp280=
XM_011517135.2:c.893_899delinsATGGTGT	XP_011515437.1:p.Asp298=
XM_011517136.2:c.839_845delinsATGGTGT	XP_011515438.1:p.Asp280=
XM_017013588.1:c.1001_1007delinsATGGTGT	XP_016869077.1:p.Asp334=
NM_018444.4:c.839_845delinsATGGTGT MANE Select	NP_060914.2:p.Asp280=
NM_001161780.2:c.914_920delinsATGGTGT	NP_001155252.1:p.Asp305=
NM_001161781.2:c.839_845delinsATGGTGT	NP_001155253.1:p.Asp280=
NM_001161779.2:c.914_920delinsATGGTGT	NP_001155251.1:p.Asp305=