Canonical Allele Identifier: CA2740962484
Gene: PDP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93923561dup , CM000670.2:g.93923561dup GRCh38
NC_000008.10:g.94935789dup , CM000670.1:g.94935789dup GRCh37
NC_000008.9:g.95004965dup NCBI36
NG_012233.1:g.11628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.1502dup MANE Select ENSP00000297598.4:p.Lys502Ter
ENST00000297598.4:c.1502dup ENSP00000297598.4:p.Lys502Ter
ENST00000396200.3:c.1577dup ENSP00000379503.3:p.Lys527Ter
ENST00000517764.1:c.1502dup ENSP00000430380.1:p.Lys502Ter
ENST00000520728.5:c.1502dup ENSP00000428317.1:p.Lys502Ter
NM_001161779.1:c.1577dup NP_001155251.1:p.Lys527Ter
NM_001161780.1:c.1577dup NP_001155252.1:p.Lys527Ter
NM_001161781.1:c.1502dup NP_001155253.1:p.Lys502Ter
NM_018444.3:c.1502dup NP_060914.2:p.Lys502Ter
XM_011517135.1:c.1556dup XP_011515437.1:p.Lys520Ter
XM_011517136.1:c.1502dup XP_011515438.1:p.Lys502Ter
XM_011517137.1:c.1502dup XP_011515439.1:p.Lys502Ter
XM_011517135.2:c.1556dup XP_011515437.1:p.Lys520Ter
XM_011517136.2:c.1502dup XP_011515438.1:p.Lys502Ter
XM_017013588.1:c.1664dup XP_016869077.1:p.Lys556Ter
NM_018444.4:c.1502dup MANE Select NP_060914.2:p.Lys502Ter
NM_001161780.2:c.1577dup NP_001155252.1:p.Lys527Ter
NM_001161781.2:c.1502dup NP_001155253.1:p.Lys502Ter
NM_001161779.2:c.1577dup NP_001155251.1:p.Lys527Ter