Canonical Allele Identifier: CA1803281028

Gene: PDP1

Linked Data

• dbSNP Id: rs1810356343

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923646_93923648del , CM000670.2:g.93923646_93923648del	GRCh38
NC_000008.10:g.94935874_94935876del , CM000670.1:g.94935874_94935876del	GRCh37
NC_000008.9:g.95005050_95005052del	NCBI36
NG_012233.1:g.11713_11715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1587_1589del MANE Select	ENSP00000297598.4:p.Val530del
ENST00000297598.4:c.1587_1589del	ENSP00000297598.4:p.Val530del
ENST00000396200.3:c.1662_1664del	ENSP00000379503.3:p.Val555del
ENST00000517764.1:c.1587_1589del	ENSP00000430380.1:p.Val530del
ENST00000520728.5:c.1587_1589del	ENSP00000428317.1:p.Val530del
NM_001161779.1:c.1662_1664del	NP_001155251.1:p.Val555del
NM_001161780.1:c.1662_1664del	NP_001155252.1:p.Val555del
NM_001161781.1:c.1587_1589del	NP_001155253.1:p.Val530del
NM_018444.3:c.1587_1589del	NP_060914.2:p.Val530del
XM_011517135.1:c.1641_1643del	XP_011515437.1:p.Val548del
XM_011517136.1:c.1587_1589del	XP_011515438.1:p.Val530del
XM_011517137.1:c.1587_1589del	XP_011515439.1:p.Val530del
XM_011517135.2:c.1641_1643del	XP_011515437.1:p.Val548del
XM_011517136.2:c.1587_1589del	XP_011515438.1:p.Val530del
XM_017013588.1:c.1749_1751del	XP_016869077.1:p.Val584del
NM_018444.4:c.1587_1589del MANE Select	NP_060914.2:p.Val530del
NM_001161780.2:c.1662_1664del	NP_001155252.1:p.Val555del
NM_001161781.2:c.1587_1589del	NP_001155253.1:p.Val530del
NM_001161779.2:c.1662_1664del	NP_001155251.1:p.Val555del