Canonical Allele Identifier: CA2640319396

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80210242_80210244del , CM000679.2:g.80210242_80210244del GRCh38
NC_000017.10:g.78184041_78184043del , CM000679.1:g.78184041_78184043del GRCh37
NC_000017.9:g.75798636_75798638del NCBI36
NG_008229.1:g.15163_15165del
NG_032778.1:g.45251_45253del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703570.1:n.2844+984_2844+986del (CARD14)
ENST00000326317.11:c.*214_*216del (SGSH) MANE Select ENSP00000314606.6:n.*214_*216del
ENST00000326317.10:c.*214_*216del (SGSH) ENSP00000314606.6:n.*214_*216del
ENST00000572257.5:c.551+1833_551+1835del (SGSH)
ENST00000573150.5:c.*933_*935del (SGSH) ENSP00000459280.1:n.*933_*935del
ENST00000575282.5:n.4606_4608del (SGSH)
NM_000199.3:c.*214_*216del (SGSH) NP_000190.1:n.*214_*216del
XM_005257583.3:c.949+1833_949+1835del (SGSH) XP_005257640.1:n.949+1833_949+1835del
NM_000199.4:c.*214_*216del (SGSH) NP_000190.1:n.*214_*216del
NM_001352921.1:c.*810_*812del (SGSH) NP_001339850.1:n.*810_*812del
NM_001352922.1:c.*773_*775del (SGSH) NP_001339851.1:n.*773_*775del
NR_148201.1:n.1704_1706del (SGSH)
XM_005257583.4:c.949+1833_949+1835del (SGSH) XP_005257640.1:n.949+1833_949+1835del
XM_017024952.1:c.*1627_*1629del (SGSH) XP_016880441.1:n.*1627_*1629del
XR_001752585.1:n.1743_1745del (SGSH)
XR_001752586.1:n.969+1833_969+1835del (SGSH)
XR_001752587.1:n.969+1833_969+1835del (SGSH)
XR_001752588.1:n.969+1833_969+1835del (SGSH)
XR_001752589.1:n.969+1833_969+1835del (SGSH)
XR_001752590.1:n.969+1833_969+1835del (SGSH)
XR_001752591.1:n.969+1833_969+1835del (SGSH)
XR_001752592.1:n.969+1833_969+1835del (SGSH)
XR_002958057.1:n.1024+1631_1024+1633del (SGSH)
NM_000199.5:c.*214_*216del (SGSH) MANE Select NP_000190.1:n.*214_*216del
NM_001352921.2:c.*810_*812del (SGSH) NP_001339850.1:n.*810_*812del
NM_001352922.2:c.*773_*775del (SGSH) NP_001339851.1:n.*773_*775del
NR_148201.2:n.1637_1639del (SGSH)
NM_001352921.3:c.*810_*812del (SGSH) NP_001339850.1:n.*810_*812del