Canonical Allele Identifier: CA2640319167

Gene: CARD14 SGSH

Linked Data

• gnomAD v4: 17-80210157-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210158del , CM000679.2:g.80210158del	GRCh38
NC_000017.10:g.78183957del , CM000679.1:g.78183957del	GRCh37
NC_000017.9:g.75798552del	NCBI36
NG_008229.1:g.15243del
NG_032778.1:g.45167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+900del (CARD14)
ENST00000326317.11:c.*294del (SGSH) MANE Select	ENSP00000314606.6:n.*294del
ENST00000326317.10:c.*294del (SGSH)	ENSP00000314606.6:n.*294del
ENST00000572257.5:c.551+1913del (SGSH)
ENST00000573150.5:c.*1013del (SGSH)	ENSP00000459280.1:n.*1013del
ENST00000575282.5:n.4686del (SGSH)
NM_000199.3:c.*294del (SGSH)	NP_000190.1:n.*294del
XM_005257583.3:c.949+1913del (SGSH)	XP_005257640.1:n.949+1913del
NM_000199.4:c.*294del (SGSH)	NP_000190.1:n.*294del
NM_001352921.1:c.*890del (SGSH)	NP_001339850.1:n.*890del
NM_001352922.1:c.*853del (SGSH)	NP_001339851.1:n.*853del
NR_148201.1:n.1784del (SGSH)
XM_005257583.4:c.949+1913del (SGSH)	XP_005257640.1:n.949+1913del
XM_017024952.1:c.*1707del (SGSH)	XP_016880441.1:n.*1707del
XR_001752585.1:n.1823del (SGSH)
XR_001752586.1:n.969+1913del (SGSH)
XR_001752587.1:n.969+1913del (SGSH)
XR_001752588.1:n.969+1913del (SGSH)
XR_001752589.1:n.969+1913del (SGSH)
XR_001752590.1:n.969+1913del (SGSH)
XR_001752591.1:n.969+1913del (SGSH)
XR_001752592.1:n.969+1913del (SGSH)
XR_002958057.1:n.1024+1711del (SGSH)
NM_000199.5:c.*294del (SGSH) MANE Select	NP_000190.1:n.*294del
NM_001352921.2:c.*890del (SGSH)	NP_001339850.1:n.*890del
NM_001352922.2:c.*853del (SGSH)	NP_001339851.1:n.*853del
NR_148201.2:n.1717del (SGSH)
NM_001352921.3:c.*890del (SGSH)	NP_001339850.1:n.*890del