Canonical Allele Identifier: CA2580615728
Gene: LTBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65551578_65551580del , CM000673.2:g.65551578_65551580del GRCh38
NC_000011.9:g.65319049_65319051del , CM000673.1:g.65319049_65319051del GRCh37
NC_000011.8:g.65075625_65075627del NCBI36
NG_016437.1:g.11654_11656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000526825.6:c.*795-11_*795-9del ENSP00000435146.2:n.*795-11_*795-9del
ENST00000526927.6:c.677-11_677-9del ENSP00000431219.2:n.677-11_677-9del
ENST00000530866.6:c.1265-11_1265-9del ENSP00000435276.2:n.1265-11_1265-9del
ENST00000689505.1:c.1409-11_1409-9del ENSP00000510401.1:n.1409-11_1409-9del
ENST00000301873.11:c.1532-11_1532-9del MANE Select ENSP00000301873.5:n.1532-11_1532-9del
ENST00000301873.9:c.1532-11_1532-9del ENSP00000301873.5:n.1532-11_1532-9del
ENST00000322147.8:c.1532-11_1532-9del ENSP00000326647.4:n.1532-11_1532-9del
ENST00000526927.5:c.483-11_483-9del
ENST00000527792.5:n.860_862del
ENST00000528516.5:c.*1177-11_*1177-9del ENSP00000432350.1:n.*1177-11_*1177-9del
ENST00000528966.5:n.205_207del
ENST00000529764.1:n.302_304del
ENST00000530866.5:c.1265-11_1265-9del ENSP00000435276.1:n.1265-11_1265-9del
ENST00000536982.5:c.-1460-11_-1460-9del ENSP00000441912.2:n.-1460-11_-1460-9del
NM_001130144.2:c.1532-11_1532-9del NP_001123616.1:n.1532-11_1532-9del
NM_001164266.1:c.1181-11_1181-9del NP_001157738.1:n.1181-11_1181-9del
NM_021070.4:c.1532-11_1532-9del NP_066548.2:n.1532-11_1532-9del
XM_011545032.1:c.1559-11_1559-9del XP_011543334.1:n.1559-11_1559-9del
XM_011545033.1:c.1559-11_1559-9del XP_011543335.1:n.1559-11_1559-9del
XR_949928.1:n.1959-11_1959-9del
XM_011545032.2:c.1559-11_1559-9del XP_011543334.1:n.1559-11_1559-9del
XM_011545033.3:c.1559-11_1559-9del XP_011543335.1:n.1559-11_1559-9del
XM_017017737.2:c.1559-11_1559-9del XP_016873226.1:n.1559-11_1559-9del
XR_001747875.2:n.1982-11_1982-9del
XR_949928.3:n.1982-11_1982-9del
NM_001130144.3:c.1532-11_1532-9del MANE Select NP_001123616.1:n.1532-11_1532-9del