Canonical Allele Identifier: CA2577269641
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2582384
ClinVar RCV Id: RCV003333365

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.230177609_230177614del , CM000664.2:g.230177609_230177614del GRCh38
NC_000002.11:g.231042325_231042330del , CM000664.1:g.231042325_231042330del GRCh37
NC_000002.10:g.230750569_230750574del NCBI36
NG_008295.1:g.47504_47509del , LRG_109:g.47504_47509del

Transcript Alleles

HGVS Amino-acid Change
ENST00000462232.2:c.911_916del ENSP00000513566.1:p.Lys304_Gly305del
ENST00000489597.2:c.1520_1525del ENSP00000513565.1:p.Lys507_Gly508del
ENST00000698099.1:c.1520_1525del ENSP00000513563.1:p.Lys507_Gly508del
ENST00000698100.1:c.1370_1375del ENSP00000513564.1:p.Lys457_Gly458del
ENST00000698101.1:n.242_247del
ENST00000698102.1:n.2336_2341del
ENST00000698103.1:c.1370_1375del ENSP00000513567.1:p.Lys457_Gly458del
ENST00000258381.11:c.1520_1525del MANE Select ENSP00000258381.6:p.Lys507_Gly508del
ENST00000258382.10:c.1520_1525del ENSP00000258382.5:p.Lys507_Gly508del
ENST00000358662.9:c.1520_1525del ENSP00000351488.4:p.Lys507_Gly508del
ENST00000540870.5:c.1538_1543del ENSP00000439558.1:p.Lys513_Gly514del
ENST00000258381.10:c.1520_1525del ENSP00000258381.6:p.Lys507_Gly508del
ENST00000258382.9:c.1520_1525del ENSP00000258382.5:p.Lys507_Gly508del
ENST00000358662.8:c.1520_1525del ENSP00000351488.4:p.Lys507_Gly508del
ENST00000392048.7:c.1514_1519del ENSP00000375902.3:p.Lys505_Gly506del
ENST00000489597.1:n.174_179del
ENST00000540870.4:c.1538_1543del ENSP00000439558.1:p.Lys513_Gly514del
NM_001185015.1:c.1538_1543del NP_001171944.1:p.Lys513_Gly514del
NM_004509.3:c.1520_1525del NP_004500.3:p.Lys507_Gly508del
NM_004510.3:c.1520_1525del NP_004501.3:p.Lys507_Gly508del
NM_080424.2:c.1520_1525del , LRG_109t1:c.1520_1525del NP_536349.2:p.Lys507_Gly508del
XM_005246525.2:c.1538_1543del XP_005246582.1:p.Lys513_Gly514del
XM_006712487.2:c.1538_1543del XP_006712550.1:p.Lys513_Gly514del
XM_006712489.2:c.1538_1543del XP_006712552.1:p.Lys513_Gly514del
XM_011511088.1:c.1538_1543del XP_011509390.1:p.Lys513_Gly514del
XM_011511089.1:c.1520_1525del XP_011509391.1:p.Lys507_Gly508del
XM_011511090.1:c.1388_1393del XP_011509392.1:p.Lys463_Gly464del
XM_011511091.1:c.1538_1543del XP_011509393.1:p.Lys513_Gly514del
XM_011511092.1:c.911_916del XP_011509394.1:p.Lys304_Gly305del
XM_005246525.4:c.1538_1543del XP_005246582.1:p.Lys513_Gly514del
XM_006712487.3:c.1538_1543del XP_006712550.1:p.Lys513_Gly514del
XM_006712489.4:c.1538_1543del XP_006712552.1:p.Lys513_Gly514del
XM_011511088.3:c.1538_1543del XP_011509390.1:p.Lys513_Gly514del
XM_011511089.3:c.1520_1525del XP_011509391.1:p.Lys507_Gly508del
XM_011511090.3:c.1388_1393del XP_011509392.1:p.Lys463_Gly464del
XM_011511091.3:c.1538_1543del XP_011509393.1:p.Lys513_Gly514del
XM_011511092.3:c.911_916del XP_011509394.1:p.Lys304_Gly305del
XM_017003968.2:c.1538_1543del XP_016859457.1:p.Lys513_Gly514del
XM_017003969.1:c.1388_1393del XP_016859458.1:p.Lys463_Gly464del
XM_024452850.1:c.1388_1393del XP_024308618.1:p.Lys463_Gly464del
XM_024452851.1:c.1370_1375del XP_024308619.1:p.Lys457_Gly458del
NM_001185015.2:c.1538_1543del NP_001171944.1:p.Lys513_Gly514del
NM_004509.4:c.1520_1525del NP_004500.4:p.Lys507_Gly508del
NM_004510.4:c.1520_1525del NP_004501.4:p.Lys507_Gly508del
NM_080424.3:c.1520_1525del NP_536349.3:p.Lys507_Gly508del
NM_001378442.1:c.1538_1543del NP_001365371.1:p.Lys513_Gly514del
NM_001378443.1:c.1520_1525del NP_001365372.1:p.Lys507_Gly508del
NM_001378444.1:c.1538_1543del NP_001365373.1:p.Lys513_Gly514del
NM_001378445.1:c.1538_1543del NP_001365374.1:p.Lys513_Gly514del
NM_001378446.1:c.1538_1543del NP_001365375.1:p.Lys513_Gly514del
NM_001378447.1:c.1370_1375del NP_001365376.1:p.Lys457_Gly458del
NM_004509.5:c.1520_1525del NP_004500.4:p.Lys507_Gly508del
NM_080424.4:c.1520_1525del MANE Select NP_536349.3:p.Lys507_Gly508del