Canonical Allele Identifier: CA357736777

Gene: PDLIM5

Linked Data

• dbSNP Id: rs13107595
• MyVariant Identifiers: chr4:g.95578588G>C (hg19) ; chr4:g.94657437G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.94657437G>C , CM000666.2:g.94657437G>C	GRCh38
NC_000004.11:g.95578588G>C , CM000666.1:g.95578588G>C	GRCh37
NC_000004.10:g.95797611G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317968.9:c.1475G>C MANE Select	ENSP00000321746.4:p.Ser492Thr
ENST00000317968.8:c.1475G>C	ENSP00000321746.4:p.Ser492Thr
ENST00000380176.7:n.1368G>C
ENST00000437932.5:c.500G>C	ENSP00000398469.2:p.Ser167Thr
ENST00000503974.5:c.1166G>C	ENSP00000424297.1:p.Ser389Thr
ENST00000506632.2:c.797G>C
ENST00000514743.5:c.1562G>C	ENSP00000424360.1:p.Ser521Thr
ENST00000542407.5:c.1148G>C	ENSP00000442187.2:p.Ser383Thr
ENST00000615540.4:c.1562G>C	ENSP00000480359.1:p.Ser521Thr
ENST00000627587.2:c.*1203G>C	ENSP00000486938.1:n.*1203G>C
NM_001011513.3:c.1148G>C	NP_001011513.3:p.Ser383Thr
NM_001256425.1:c.500G>C	NP_001243354.1:p.Ser167Thr
NM_001256426.1:c.1562G>C	NP_001243355.1:p.Ser521Thr
NM_001256427.1:c.1166G>C	NP_001243356.1:p.Ser389Thr
NM_001256428.1:c.1109G>C	NP_001243357.1:p.Ser370Thr
NM_006457.4:c.1475G>C	NP_006448.4:p.Ser492Thr
XM_005262693.3:c.1889G>C	XP_005262750.1:p.Ser630Thr
XM_005262695.3:c.1871G>C	XP_005262752.1:p.Ser624Thr
XM_005262696.3:c.1544G>C	XP_005262753.1:p.Ser515Thr
XM_005262698.3:c.1166G>C	XP_005262755.1:p.Ser389Thr
XM_006714066.2:c.1904G>C	XP_006714129.1:p.Ser635Thr
XM_006714067.2:c.1904G>C	XP_006714130.1:p.Ser635Thr
XM_006714068.2:c.1577G>C	XP_006714131.1:p.Ser526Thr
XM_006714069.2:c.1508G>C	XP_006714132.1:p.Ser503Thr
XM_006714070.2:c.1502G>C	XP_006714133.1:p.Ser501Thr
XM_011531543.1:c.1487G>C	XP_011529845.1:p.Ser496Thr
XM_005262693.5:c.1889G>C	XP_005262750.1:p.Ser630Thr
XM_005262695.5:c.1871G>C	XP_005262752.1:p.Ser624Thr
XM_005262696.4:c.1544G>C	XP_005262753.1:p.Ser515Thr
XM_005262698.4:c.1166G>C	XP_005262755.1:p.Ser389Thr
XM_006714066.4:c.1904G>C	XP_006714129.1:p.Ser635Thr
XM_006714068.3:c.1577G>C	XP_006714131.1:p.Ser526Thr
XM_006714069.4:c.1508G>C	XP_006714132.1:p.Ser503Thr
XM_006714070.3:c.1502G>C	XP_006714133.1:p.Ser501Thr
XM_011531543.3:c.1487G>C	XP_011529845.1:p.Ser496Thr
XM_017007657.2:c.1493G>C	XP_016863146.1:p.Ser498Thr
XM_017007658.1:c.1181G>C	XP_016863147.1:p.Ser394Thr
NM_001011513.4:c.1148G>C	NP_001011513.4:p.Ser383Thr
NM_001256427.2:c.1166G>C	NP_001243356.2:p.Ser389Thr
NM_001256428.2:c.1109G>C	NP_001243357.2:p.Ser370Thr
NM_006457.5:c.1475G>C MANE Select	NP_006448.5:p.Ser492Thr
NM_001256425.2:c.500G>C	NP_001243354.2:p.Ser167Thr
NM_001256426.2:c.1562G>C	NP_001243355.2:p.Ser521Thr