Canonical Allele Identifier: CA553453611

Gene: PDLIM5

Linked Data

• dbSNP Id: rs1390894807
• gnomAD v2: 4-95579738-TAGA-T
• gnomAD v3: 4-94658587-TAGA-T
• gnomAD v4: 4-94658587-TAGA-T
• MyVariant Identifiers: chr4:g.95579739_95579741del (hg19) ; chr4:g.94658588_94658590del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.94658590_94658592del , CM000666.2:g.94658590_94658592del	GRCh38
NC_000004.11:g.95579741_95579743del , CM000666.1:g.95579741_95579743del	GRCh37
NC_000004.10:g.95798764_95798766del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317968.9:c.1585+1043_1585+1045del MANE Select	ENSP00000321746.4:n.1585+1043_1585+1045del
ENST00000317968.8:c.1585+1043_1585+1045del	ENSP00000321746.4:n.1585+1043_1585+1045del
ENST00000380176.7:n.1478+1043_1478+1045del
ENST00000437932.5:c.610+1043_610+1045del	ENSP00000398469.2:n.610+1043_610+1045del
ENST00000503974.5:c.1276+1043_1276+1045del	ENSP00000424297.1:n.1276+1043_1276+1045del
ENST00000514743.5:c.1672+1043_1672+1045del	ENSP00000424360.1:n.1672+1043_1672+1045del
ENST00000542407.5:c.1258+1043_1258+1045del	ENSP00000442187.2:n.1258+1043_1258+1045del
ENST00000615540.4:c.1672+1043_1672+1045del	ENSP00000480359.1:n.1672+1043_1672+1045del
ENST00000627587.2:c.*1313+1043_*1313+1045del	ENSP00000486938.1:n.*1313+1043_*1313+1045del
NM_001011513.3:c.1258+1043_1258+1045del	NP_001011513.3:n.1258+1043_1258+1045del
NM_001256425.1:c.610+1043_610+1045del	NP_001243354.1:n.610+1043_610+1045del
NM_001256426.1:c.1672+1043_1672+1045del	NP_001243355.1:n.1672+1043_1672+1045del
NM_001256427.1:c.1276+1043_1276+1045del	NP_001243356.1:n.1276+1043_1276+1045del
NM_001256428.1:c.1219+1043_1219+1045del	NP_001243357.1:n.1219+1043_1219+1045del
NM_006457.4:c.1585+1043_1585+1045del	NP_006448.4:n.1585+1043_1585+1045del
XM_005262693.3:c.1999+1043_1999+1045del	XP_005262750.1:n.1999+1043_1999+1045del
XM_005262695.3:c.1981+1043_1981+1045del	XP_005262752.1:n.1981+1043_1981+1045del
XM_005262696.3:c.1654+1043_1654+1045del	XP_005262753.1:n.1654+1043_1654+1045del
XM_005262698.3:c.1276+1043_1276+1045del	XP_005262755.1:n.1276+1043_1276+1045del
XM_006714066.2:c.2014+1043_2014+1045del	XP_006714129.1:n.2014+1043_2014+1045del
XM_006714067.2:c.2014+1043_2014+1045del	XP_006714130.1:n.2014+1043_2014+1045del
XM_006714068.2:c.1687+1043_1687+1045del	XP_006714131.1:n.1687+1043_1687+1045del
XM_006714069.2:c.1618+1043_1618+1045del	XP_006714132.1:n.1618+1043_1618+1045del
XM_006714070.2:c.1612+1043_1612+1045del	XP_006714133.1:n.1612+1043_1612+1045del
XM_011531543.1:c.1597+1043_1597+1045del	XP_011529845.1:n.1597+1043_1597+1045del
XM_005262693.5:c.1999+1043_1999+1045del	XP_005262750.1:n.1999+1043_1999+1045del
XM_005262695.5:c.1981+1043_1981+1045del	XP_005262752.1:n.1981+1043_1981+1045del
XM_005262696.4:c.1654+1043_1654+1045del	XP_005262753.1:n.1654+1043_1654+1045del
XM_005262698.4:c.1276+1043_1276+1045del	XP_005262755.1:n.1276+1043_1276+1045del
XM_006714066.4:c.2014+1043_2014+1045del	XP_006714129.1:n.2014+1043_2014+1045del
XM_006714068.3:c.1687+1043_1687+1045del	XP_006714131.1:n.1687+1043_1687+1045del
XM_006714069.4:c.1618+1043_1618+1045del	XP_006714132.1:n.1618+1043_1618+1045del
XM_006714070.3:c.1612+1043_1612+1045del	XP_006714133.1:n.1612+1043_1612+1045del
XM_011531543.3:c.1597+1043_1597+1045del	XP_011529845.1:n.1597+1043_1597+1045del
XM_017007657.2:c.1603+1043_1603+1045del	XP_016863146.1:n.1603+1043_1603+1045del
XM_017007658.1:c.1291+1043_1291+1045del	XP_016863147.1:n.1291+1043_1291+1045del
NM_001011513.4:c.1258+1043_1258+1045del	NP_001011513.4:n.1258+1043_1258+1045del
NM_001256427.2:c.1276+1043_1276+1045del	NP_001243356.2:n.1276+1043_1276+1045del
NM_001256428.2:c.1219+1043_1219+1045del	NP_001243357.2:n.1219+1043_1219+1045del
NM_006457.5:c.1585+1043_1585+1045del MANE Select	NP_006448.5:n.1585+1043_1585+1045del
NM_001256425.2:c.610+1043_610+1045del	NP_001243354.2:n.610+1043_610+1045del
NM_001256426.2:c.1672+1043_1672+1045del	NP_001243355.2:n.1672+1043_1672+1045del