Canonical Allele Identifier: CA371694398
Gene: PDP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93922895T>C , CM000670.2:g.93922895T>C GRCh38
NC_000008.10:g.94935123T>C , CM000670.1:g.94935123T>C GRCh37
NC_000008.9:g.95004299T>C NCBI36
NG_012233.1:g.10962T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297598.5:c.836T>C MANE Select ENSP00000297598.4:p.Val279Ala
ENST00000297598.4:c.836T>C ENSP00000297598.4:p.Val279Ala
ENST00000396200.3:c.911T>C ENSP00000379503.3:p.Val304Ala
ENST00000517764.1:c.836T>C ENSP00000430380.1:p.Val279Ala
ENST00000520728.5:c.836T>C ENSP00000428317.1:p.Val279Ala
NM_001161779.1:c.911T>C NP_001155251.1:p.Val304Ala
NM_001161780.1:c.911T>C NP_001155252.1:p.Val304Ala
NM_001161781.1:c.836T>C NP_001155253.1:p.Val279Ala
NM_018444.3:c.836T>C NP_060914.2:p.Val279Ala
XM_011517135.1:c.890T>C XP_011515437.1:p.Val297Ala
XM_011517136.1:c.836T>C XP_011515438.1:p.Val279Ala
XM_011517137.1:c.836T>C XP_011515439.1:p.Val279Ala
XM_011517135.2:c.890T>C XP_011515437.1:p.Val297Ala
XM_011517136.2:c.836T>C XP_011515438.1:p.Val279Ala
XM_017013588.1:c.998T>C XP_016869077.1:p.Val333Ala
NM_018444.4:c.836T>C MANE Select NP_060914.2:p.Val279Ala
NM_001161780.2:c.911T>C NP_001155252.1:p.Val304Ala
NM_001161781.2:c.836T>C NP_001155253.1:p.Val279Ala
NM_001161779.2:c.911T>C NP_001155251.1:p.Val304Ala