Canonical Allele Identifier: CA1477719265
Gene: PDLIM5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94618116G= , CM000666.2:g.94618116G= GRCh38
NC_000004.11:g.95539267G= , CM000666.1:g.95539267G= GRCh37
NC_000004.10:g.95758290G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006457.5:c.1033G= MANE Select NP_006448.5:p.Ala345=
ENST00000317968.9:c.1033G= MANE Select ENSP00000321746.4:p.Ala345=
NM_001011513.4:c.706G= NP_001011513.4:p.Ala236=
NM_001256425.2:c.58G= NP_001243354.2:p.Ala20=
NM_001256426.2:c.1120G= NP_001243355.2:p.Ala374=
NM_001256427.2:c.724G= NP_001243356.2:p.Ala242=
NM_001256428.2:c.667G= NP_001243357.2:p.Ala223=
ENST00000317968.8:c.1033G= ENSP00000321746.4:p.Ala345=
ENST00000380176.7:n.926G=
ENST00000437932.5:c.58G= ENSP00000398469.2:p.Ala20=
ENST00000503974.5:c.724G= ENSP00000424297.1:p.Ala242=
ENST00000506632.2:c.261G=
ENST00000509357.5:c.518G= ENSP00000422833.1:n.518G=
ENST00000511586.5:n.472G=
ENST00000514743.5:c.1120G= ENSP00000424360.1:p.Ala374=
ENST00000542407.5:c.706G= ENSP00000442187.2:p.Ala236=
ENST00000615540.4:c.1120G= ENSP00000480359.1:p.Ala374=
ENST00000627587.2:c.*761G= ENSP00000486938.1:n.*761G=
XM_005262693.3:c.1447G= XP_005262750.1:p.Ala483=
XM_005262693.5:c.1447G= XP_005262750.1:p.Ala483=
XM_005262695.3:c.1429G= XP_005262752.1:p.Ala477=
XM_005262695.5:c.1429G= XP_005262752.1:p.Ala477=
XM_005262696.3:c.1102G= XP_005262753.1:p.Ala368=
XM_005262696.4:c.1102G= XP_005262753.1:p.Ala368=
XM_005262698.3:c.724G= XP_005262755.1:p.Ala242=
XM_005262698.4:c.724G= XP_005262755.1:p.Ala242=
XM_006714066.2:c.1462G= XP_006714129.1:p.Ala488=
XM_006714066.4:c.1462G= XP_006714129.1:p.Ala488=
XM_006714067.2:c.1462G= XP_006714130.1:p.Ala488=
XM_006714068.2:c.1135G= XP_006714131.1:p.Ala379=
XM_006714068.3:c.1135G= XP_006714131.1:p.Ala379=
XM_006714069.2:c.1066G= XP_006714132.1:p.Ala356=
XM_006714069.4:c.1066G= XP_006714132.1:p.Ala356=
XM_006714070.2:c.1060G= XP_006714133.1:p.Ala354=
XM_006714070.3:c.1060G= XP_006714133.1:p.Ala354=
XM_011531543.1:c.1045G= XP_011529845.1:p.Ala349=
XM_011531543.3:c.1045G= XP_011529845.1:p.Ala349=
XM_017007657.2:c.1051G= XP_016863146.1:p.Ala351=
XM_017007658.1:c.739G= XP_016863147.1:p.Ala247=