Canonical Allele Identifier: CA2277863809

Gene: CARD14 SGSH

Linked Data

• dbSNP Id: rs2041765982

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80213751_80213752insATAATCCAT , CM000679.2:g.80213751_80213752insATAATCCAT	GRCh38
NC_000017.10:g.78187550_78187551insATAATCCAT , CM000679.1:g.78187550_78187551insATAATCCAT	GRCh37
NC_000017.9:g.75802145_75802146insATAATCCAT	NCBI36
NG_008229.1:g.11649_11650insATGGATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-2115_2845-2114insATAATCCAT (CARD14)
ENST00000326317.11:c.745+52_745+53insATGGATTAT (SGSH) MANE Select	ENSP00000314606.6:n.745+52_745+53insATGGATTAT
ENST00000326317.10:c.745+52_745+53insATGGATTAT (SGSH)	ENSP00000314606.6:n.745+52_745+53insATGGATTAT
ENST00000570923.1:c.780+52_780+53insATGGATTAT (SGSH)	ENSP00000458200.1:n.780+52_780+53insATGGATTAT
ENST00000572257.5:c.347+52_347+53insATGGATTAT (SGSH)
ENST00000573150.5:c.639+52_639+53insATGGATTAT (SGSH)	ENSP00000459280.1:n.639+52_639+53insATGGATTAT
ENST00000575282.5:n.1092_1093insATGGATTAT (SGSH)
ENST00000576941.5:c.*161+52_*161+53insATGGATTAT (SGSH)	ENSP00000461160.1:n.*161+52_*161+53insATGGATTAT
NM_000199.3:c.745+52_745+53insATGGATTAT (SGSH)	NP_000190.1:n.745+52_745+53insATGGATTAT
XM_005257582.2:c.745+52_745+53insATGGATTAT (SGSH)	XP_005257639.1:n.745+52_745+53insATGGATTAT
XM_005257583.3:c.745+52_745+53insATGGATTAT (SGSH)	XP_005257640.1:n.745+52_745+53insATGGATTAT
XM_011525126.1:c.745+52_745+53insATGGATTAT (SGSH)	XP_011523428.1:n.745+52_745+53insATGGATTAT
XM_011525127.1:c.745+52_745+53insATGGATTAT (SGSH)	XP_011523429.1:n.745+52_745+53insATGGATTAT
XR_934532.1:n.765+52_765+53insATGGATTAT (SGSH)
NM_000199.4:c.745+52_745+53insATGGATTAT (SGSH)	NP_000190.1:n.745+52_745+53insATGGATTAT
NM_001352921.1:c.745+52_745+53insATGGATTAT (SGSH)	NP_001339850.1:n.745+52_745+53insATGGATTAT
NM_001352922.1:c.745+52_745+53insATGGATTAT (SGSH)	NP_001339851.1:n.745+52_745+53insATGGATTAT
NR_148201.1:n.726+52_726+53insATGGATTAT (SGSH)
XM_005257583.4:c.745+52_745+53insATGGATTAT (SGSH)	XP_005257640.1:n.745+52_745+53insATGGATTAT
XM_017024952.1:c.745+52_745+53insATGGATTAT (SGSH)	XP_016880441.1:n.745+52_745+53insATGGATTAT
XR_001752585.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752586.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752587.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752588.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752589.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752590.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752591.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_001752592.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_002958057.1:n.765+52_765+53insATGGATTAT (SGSH)
XR_934532.2:n.765+52_765+53insATGGATTAT (SGSH)
NM_000199.5:c.745+52_745+53insATGGATTAT (SGSH) MANE Select	NP_000190.1:n.745+52_745+53insATGGATTAT
NM_001352921.2:c.745+52_745+53insATGGATTAT (SGSH)	NP_001339850.1:n.745+52_745+53insATGGATTAT
NM_001352922.2:c.745+52_745+53insATGGATTAT (SGSH)	NP_001339851.1:n.745+52_745+53insATGGATTAT
NR_148201.2:n.659+52_659+53insATGGATTAT (SGSH)
NM_001352921.3:c.745+52_745+53insATGGATTAT (SGSH)	NP_001339850.1:n.745+52_745+53insATGGATTAT