Canonical Allele Identifier: CA3014598

Gene: PDLIM5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317968.9:c.1033G>A MANE Select	ENSP00000321746.4:p.Ala345Thr
ENST00000317968.8:c.1033G>A	ENSP00000321746.4:p.Ala345Thr
ENST00000380176.7:n.926G>A
ENST00000437932.5:c.58G>A	ENSP00000398469.2:p.Ala20Thr
ENST00000503974.5:c.724G>A	ENSP00000424297.1:p.Ala242Thr
ENST00000506632.2:c.261G>A
ENST00000509357.5:c.518G>A	ENSP00000422833.1:n.518G>A
ENST00000511586.5:n.472G>A
ENST00000514743.5:c.1120G>A	ENSP00000424360.1:p.Ala374Thr
ENST00000542407.5:c.706G>A	ENSP00000442187.2:p.Ala236Thr
ENST00000615540.4:c.1120G>A	ENSP00000480359.1:p.Ala374Thr
ENST00000627587.2:c.*761G>A	ENSP00000486938.1:n.*761G>A
XM_005262693.3:c.1447G>A	XP_005262750.1:p.Ala483Thr
XM_005262695.3:c.1429G>A	XP_005262752.1:p.Ala477Thr
XM_005262696.3:c.1102G>A	XP_005262753.1:p.Ala368Thr
XM_005262698.3:c.724G>A	XP_005262755.1:p.Ala242Thr
XM_006714066.2:c.1462G>A	XP_006714129.1:p.Ala488Thr
XM_006714067.2:c.1462G>A	XP_006714130.1:p.Ala488Thr
XM_006714068.2:c.1135G>A	XP_006714131.1:p.Ala379Thr
XM_006714069.2:c.1066G>A	XP_006714132.1:p.Ala356Thr
XM_006714070.2:c.1060G>A	XP_006714133.1:p.Ala354Thr
XM_011531543.1:c.1045G>A	XP_011529845.1:p.Ala349Thr
XM_005262693.5:c.1447G>A	XP_005262750.1:p.Ala483Thr
XM_005262695.5:c.1429G>A	XP_005262752.1:p.Ala477Thr
XM_005262696.4:c.1102G>A	XP_005262753.1:p.Ala368Thr
XM_005262698.4:c.724G>A	XP_005262755.1:p.Ala242Thr
XM_006714066.4:c.1462G>A	XP_006714129.1:p.Ala488Thr
XM_006714068.3:c.1135G>A	XP_006714131.1:p.Ala379Thr
XM_006714069.4:c.1066G>A	XP_006714132.1:p.Ala356Thr
XM_006714070.3:c.1060G>A	XP_006714133.1:p.Ala354Thr
XM_011531543.3:c.1045G>A	XP_011529845.1:p.Ala349Thr
XM_017007657.2:c.1051G>A	XP_016863146.1:p.Ala351Thr
XM_017007658.1:c.739G>A	XP_016863147.1:p.Ala247Thr
NM_001011513.4:c.706G>A	NP_001011513.4:p.Ala236Thr
NM_001256427.2:c.724G>A	NP_001243356.2:p.Ala242Thr
NM_001256428.2:c.667G>A	NP_001243357.2:p.Ala223Thr
NM_006457.5:c.1033G>A MANE Select	NP_006448.5:p.Ala345Thr
NM_001256425.2:c.58G>A	NP_001243354.2:p.Ala20Thr
NM_001256426.2:c.1120G>A	NP_001243355.2:p.Ala374Thr