Canonical Allele Identifier: CA1477729125

Gene: PDLIM5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.94640308A= , CM000666.2:g.94640308A=	GRCh38
NC_000004.11:g.95561459A= , CM000666.1:g.95561459A=	GRCh37
NC_000004.10:g.95780482A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006457.5:c.1141A= MANE Select	NP_006448.5:p.Thr381=
ENST00000317968.9:c.1141A= MANE Select	ENSP00000321746.4:p.Thr381=
NM_001011513.3:c.814A=	NP_001011513.3:p.Thr272=
NM_001011513.4:c.814A=	NP_001011513.4:p.Thr272=
NM_001256425.1:c.166A=	NP_001243354.1:p.Thr56=
NM_001256425.2:c.166A=	NP_001243354.2:p.Thr56=
NM_001256426.1:c.1228A=	NP_001243355.1:p.Thr410=
NM_001256426.2:c.1228A=	NP_001243355.2:p.Thr410=
NM_001256427.1:c.832A=	NP_001243356.1:p.Thr278=
NM_001256427.2:c.832A=	NP_001243356.2:p.Thr278=
NM_001256428.1:c.775A=	NP_001243357.1:p.Thr259=
NM_001256428.2:c.775A=	NP_001243357.2:p.Thr259=
NM_006457.4:c.1141A=	NP_006448.4:p.Thr381=
ENST00000317968.8:c.1141A=	ENSP00000321746.4:p.Thr381=
ENST00000380176.7:n.1034A=
ENST00000437932.5:c.166A=	ENSP00000398469.2:p.Thr56=
ENST00000503974.5:c.832A=	ENSP00000424297.1:p.Thr278=
ENST00000506632.2:c.369A=
ENST00000514743.5:c.1228A=	ENSP00000424360.1:p.Thr410=
ENST00000542407.5:c.814A=	ENSP00000442187.2:p.Thr272=
ENST00000615540.4:c.1228A=	ENSP00000480359.1:p.Thr410=
ENST00000627587.2:c.*869A=	ENSP00000486938.1:n.*869A=
XM_005262693.3:c.1555A=	XP_005262750.1:p.Thr519=
XM_005262693.5:c.1555A=	XP_005262750.1:p.Thr519=
XM_005262695.3:c.1537A=	XP_005262752.1:p.Thr513=
XM_005262695.5:c.1537A=	XP_005262752.1:p.Thr513=
XM_005262696.3:c.1210A=	XP_005262753.1:p.Thr404=
XM_005262696.4:c.1210A=	XP_005262753.1:p.Thr404=
XM_005262698.3:c.832A=	XP_005262755.1:p.Thr278=
XM_005262698.4:c.832A=	XP_005262755.1:p.Thr278=
XM_006714066.2:c.1570A=	XP_006714129.1:p.Thr524=
XM_006714066.4:c.1570A=	XP_006714129.1:p.Thr524=
XM_006714067.2:c.1570A=	XP_006714130.1:p.Thr524=
XM_006714068.2:c.1243A=	XP_006714131.1:p.Thr415=
XM_006714068.3:c.1243A=	XP_006714131.1:p.Thr415=
XM_006714069.2:c.1174A=	XP_006714132.1:p.Thr392=
XM_006714069.4:c.1174A=	XP_006714132.1:p.Thr392=
XM_006714070.2:c.1168A=	XP_006714133.1:p.Thr390=
XM_006714070.3:c.1168A=	XP_006714133.1:p.Thr390=
XM_011531543.1:c.1153A=	XP_011529845.1:p.Thr385=
XM_011531543.3:c.1153A=	XP_011529845.1:p.Thr385=
XM_017007657.2:c.1159A=	XP_016863146.1:p.Thr387=
XM_017007658.1:c.847A=	XP_016863147.1:p.Thr283=