Canonical Allele Identifier: CA11653805

Gene: PDLIM5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.94651548C>T , CM000666.2:g.94651548C>T	GRCh38
NC_000004.11:g.95572699C>T , CM000666.1:g.95572699C>T	GRCh37
NC_000004.10:g.95791722C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317968.9:c.1284-2912C>T MANE Select	ENSP00000321746.4:n.1284-2912C>T
ENST00000317968.8:c.1284-2912C>T	ENSP00000321746.4:n.1284-2912C>T
ENST00000380176.7:n.1177-2912C>T
ENST00000437932.5:c.309-2912C>T	ENSP00000398469.2:n.309-2912C>T
ENST00000503974.5:c.975-2912C>T	ENSP00000424297.1:n.975-2912C>T
ENST00000506632.2:c.512-2912C>T
ENST00000514743.5:c.1371-2912C>T	ENSP00000424360.1:n.1371-2912C>T
ENST00000542407.5:c.957-2912C>T	ENSP00000442187.2:n.957-2912C>T
ENST00000615540.4:c.1371-2912C>T	ENSP00000480359.1:n.1371-2912C>T
ENST00000627587.2:c.*1012-2912C>T	ENSP00000486938.1:n.*1012-2912C>T
NM_001011513.3:c.957-2912C>T	NP_001011513.3:n.957-2912C>T
NM_001256425.1:c.309-2912C>T	NP_001243354.1:n.309-2912C>T
NM_001256426.1:c.1371-2912C>T	NP_001243355.1:n.1371-2912C>T
NM_001256427.1:c.975-2912C>T	NP_001243356.1:n.975-2912C>T
NM_001256428.1:c.918-2912C>T	NP_001243357.1:n.918-2912C>T
NM_006457.4:c.1284-2912C>T	NP_006448.4:n.1284-2912C>T
XM_005262693.3:c.1698-2912C>T	XP_005262750.1:n.1698-2912C>T
XM_005262695.3:c.1680-2912C>T	XP_005262752.1:n.1680-2912C>T
XM_005262696.3:c.1353-2912C>T	XP_005262753.1:n.1353-2912C>T
XM_005262698.3:c.975-2912C>T	XP_005262755.1:n.975-2912C>T
XM_006714066.2:c.1713-2912C>T	XP_006714129.1:n.1713-2912C>T
XM_006714067.2:c.1713-2912C>T	XP_006714130.1:n.1713-2912C>T
XM_006714068.2:c.1386-2912C>T	XP_006714131.1:n.1386-2912C>T
XM_006714069.2:c.1317-2912C>T	XP_006714132.1:n.1317-2912C>T
XM_006714070.2:c.1311-2912C>T	XP_006714133.1:n.1311-2912C>T
XM_011531543.1:c.1296-2912C>T	XP_011529845.1:n.1296-2912C>T
XM_005262693.5:c.1698-2912C>T	XP_005262750.1:n.1698-2912C>T
XM_005262695.5:c.1680-2912C>T	XP_005262752.1:n.1680-2912C>T
XM_005262696.4:c.1353-2912C>T	XP_005262753.1:n.1353-2912C>T
XM_005262698.4:c.975-2912C>T	XP_005262755.1:n.975-2912C>T
XM_006714066.4:c.1713-2912C>T	XP_006714129.1:n.1713-2912C>T
XM_006714068.3:c.1386-2912C>T	XP_006714131.1:n.1386-2912C>T
XM_006714069.4:c.1317-2912C>T	XP_006714132.1:n.1317-2912C>T
XM_006714070.3:c.1311-2912C>T	XP_006714133.1:n.1311-2912C>T
XM_011531543.3:c.1296-2912C>T	XP_011529845.1:n.1296-2912C>T
XM_017007657.2:c.1302-2912C>T	XP_016863146.1:n.1302-2912C>T
XM_017007658.1:c.990-2912C>T	XP_016863147.1:n.990-2912C>T
NM_001011513.4:c.957-2912C>T	NP_001011513.4:n.957-2912C>T
NM_001256427.2:c.975-2912C>T	NP_001243356.2:n.975-2912C>T
NM_001256428.2:c.918-2912C>T	NP_001243357.2:n.918-2912C>T
NM_006457.5:c.1284-2912C>T MANE Select	NP_006448.5:n.1284-2912C>T
NM_001256425.2:c.309-2912C>T	NP_001243354.2:n.309-2912C>T
NM_001256426.2:c.1371-2912C>T	NP_001243355.2:n.1371-2912C>T