Canonical Allele Identifier: CA2640319177

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80210160_80210161del , CM000679.2:g.80210160_80210161del GRCh38
NC_000017.10:g.78183959_78183960del , CM000679.1:g.78183959_78183960del GRCh37
NC_000017.9:g.75798554_75798555del NCBI36
NG_008229.1:g.15241_15242del
NG_032778.1:g.45169_45170del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703570.1:n.2844+902_2844+903del (CARD14)
ENST00000326317.11:c.*292_*293del (SGSH) MANE Select ENSP00000314606.6:n.*292_*293del
ENST00000326317.10:c.*292_*293del (SGSH) ENSP00000314606.6:n.*292_*293del
ENST00000572257.5:c.551+1911_551+1912del (SGSH)
ENST00000573150.5:c.*1011_*1012del (SGSH) ENSP00000459280.1:n.*1011_*1012del
ENST00000575282.5:n.4684_4685del (SGSH)
NM_000199.3:c.*292_*293del (SGSH) NP_000190.1:n.*292_*293del
XM_005257583.3:c.949+1911_949+1912del (SGSH) XP_005257640.1:n.949+1911_949+1912del
NM_000199.4:c.*292_*293del (SGSH) NP_000190.1:n.*292_*293del
NM_001352921.1:c.*888_*889del (SGSH) NP_001339850.1:n.*888_*889del
NM_001352922.1:c.*851_*852del (SGSH) NP_001339851.1:n.*851_*852del
NR_148201.1:n.1782_1783del (SGSH)
XM_005257583.4:c.949+1911_949+1912del (SGSH) XP_005257640.1:n.949+1911_949+1912del
XM_017024952.1:c.*1705_*1706del (SGSH) XP_016880441.1:n.*1705_*1706del
XR_001752585.1:n.1821_1822del (SGSH)
XR_001752586.1:n.969+1911_969+1912del (SGSH)
XR_001752587.1:n.969+1911_969+1912del (SGSH)
XR_001752588.1:n.969+1911_969+1912del (SGSH)
XR_001752589.1:n.969+1911_969+1912del (SGSH)
XR_001752590.1:n.969+1911_969+1912del (SGSH)
XR_001752591.1:n.969+1911_969+1912del (SGSH)
XR_001752592.1:n.969+1911_969+1912del (SGSH)
XR_002958057.1:n.1024+1709_1024+1710del (SGSH)
NM_000199.5:c.*292_*293del (SGSH) MANE Select NP_000190.1:n.*292_*293del
NM_001352921.2:c.*888_*889del (SGSH) NP_001339850.1:n.*888_*889del
NM_001352922.2:c.*851_*852del (SGSH) NP_001339851.1:n.*851_*852del
NR_148201.2:n.1715_1716del (SGSH)
NM_001352921.3:c.*888_*889del (SGSH) NP_001339850.1:n.*888_*889del