Canonical Allele Identifier: CA2830535346

Gene: PDLIM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185523193_185523194insACATCAAGAAAAA , CM000666.2:g.185523193_185523194insACATCAAGAAAAA	GRCh38
NC_000004.11:g.186444347_186444348insACATCAAGAAAAA , CM000666.1:g.186444347_186444348insACATCAAGAAAAA	GRCh37
NC_000004.10:g.186681341_186681342insACATCAAGAAAAA	NCBI36
NG_032576.2:g.17365_17366insTTTTTCTTGATGT
NG_032576.3:g.17365_17366insTTTTTCTTGATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284767.12:c.330+168_330+169insTTTTTCTTGATGT MANE Select	ENSP00000284767.8:n.330+168_330+169insTTTTTCTTGATGT
ENST00000284770.10:c.94-8857_94-8856insTTTTTCTTGATGT	ENSP00000284770.5:n.94-8857_94-8856insTTTTTCTTGATGT
ENST00000284771.7:c.330+168_330+169insTTTTTCTTGATGT	ENSP00000284771.6:n.330+168_330+169insTTTTTCTTGATGT
ENST00000620787.5:c.330+168_330+169insTTTTTCTTGATGT	ENSP00000481771.2:n.330+168_330+169insTTTTTCTTGATGT
ENST00000643009.1:c.318+168_318+169insTTTTTCTTGATGT	ENSP00000495411.1:n.318+168_318+169insTTTTTCTTGATGT
ENST00000284767.9:c.330+168_330+169insTTTTTCTTGATGT	ENSP00000284767.6:n.330+168_330+169insTTTTTCTTGATGT
ENST00000284770.9:c.330+168_330+169insTTTTTCTTGATGT	ENSP00000284770.4:n.330+168_330+169insTTTTTCTTGATGT
ENST00000284771.6:c.330+168_330+169insTTTTTCTTGATGT	ENSP00000284771.6:n.330+168_330+169insTTTTTCTTGATGT
ENST00000504011.5:n.387+168_387+169insTTTTTCTTGATGT
ENST00000504355.5:n.318+1826_318+1827insTTTTTCTTGATGT
ENST00000505886.5:c.*49+168_*49+169insTTTTTCTTGATGT	ENSP00000425138.1:n.*49+168_*49+169insTTTTTCTTGATGT
ENST00000512293.1:c.*49+168_*49+169insTTTTTCTTGATGT	ENSP00000421972.1:n.*49+168_*49+169insTTTTTCTTGATGT
ENST00000512380.1:n.188+168_188+169insTTTTTCTTGATGT
ENST00000515261.1:n.571_572insTTTTTCTTGATGT
ENST00000620787.4:c.94-8857_94-8856insTTTTTCTTGATGT	ENSP00000481771.1:n.94-8857_94-8856insTTTTTCTTGATGT
ENST00000629667.2:c.*49+168_*49+169insTTTTTCTTGATGT	ENSP00000486107.1:n.*49+168_*49+169insTTTTTCTTGATGT
NM_001114107.4:c.330+168_330+169insTTTTTCTTGATGT	NP_001107579.1:n.330+168_330+169insTTTTTCTTGATGT
NM_001257962.1:c.330+168_330+169insTTTTTCTTGATGT	NP_001244891.1:n.330+168_330+169insTTTTTCTTGATGT
NM_001257963.1:c.94-8857_94-8856insTTTTTCTTGATGT	NP_001244892.1:n.94-8857_94-8856insTTTTTCTTGATGT
NM_014476.5:c.330+168_330+169insTTTTTCTTGATGT	NP_055291.2:n.330+168_330+169insTTTTTCTTGATGT
NR_047562.1:n.454+168_454+169insTTTTTCTTGATGT
XM_011531874.1:c.330+168_330+169insTTTTTCTTGATGT	XP_011530176.1:n.330+168_330+169insTTTTTCTTGATGT
XR_938723.1:n.503+168_503+169insTTTTTCTTGATGT
XR_938724.1:n.503+168_503+169insTTTTTCTTGATGT
XR_001741206.2:n.403+168_403+169insTTTTTCTTGATGT
XR_938723.3:n.403+168_403+169insTTTTTCTTGATGT
XR_938724.3:n.403+168_403+169insTTTTTCTTGATGT
NM_001114107.5:c.330+168_330+169insTTTTTCTTGATGT	NP_001107579.1:n.330+168_330+169insTTTTTCTTGATGT
NM_014476.6:c.330+168_330+169insTTTTTCTTGATGT MANE Select	NP_055291.2:n.330+168_330+169insTTTTTCTTGATGT
NM_001257962.2:c.330+168_330+169insTTTTTCTTGATGT	NP_001244891.1:n.330+168_330+169insTTTTTCTTGATGT
NM_001257963.2:c.94-8857_94-8856insTTTTTCTTGATGT	NP_001244892.1:n.94-8857_94-8856insTTTTTCTTGATGT
NR_047562.2:n.403+168_403+169insTTTTTCTTGATGT