Canonical Allele Identifier: CA2277862278

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210656G= , CM000679.2:g.80210656G=	GRCh38
NC_000017.10:g.78184455G= , CM000679.1:g.78184455G=	GRCh37
NC_000017.9:g.75799050G=	NCBI36
NG_008229.1:g.14745C=
NG_032778.1:g.45665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1398G= (CARD14)
ENST00000326317.11:c.1305C= (SGSH) MANE Select	ENSP00000314606.6:p.Arg435=
ENST00000326317.10:c.1305C= (SGSH)	ENSP00000314606.6:p.Arg435=
ENST00000572257.5:c.551+1415C= (SGSH)
ENST00000573150.5:c.*515C= (SGSH)	ENSP00000459280.1:n.*515C=
ENST00000575282.5:n.4188C= (SGSH)
ENST00000576856.1:c.559C= (SGSH)	ENSP00000460720.1:n.559C=
NM_000199.3:c.1305C= (SGSH)	NP_000190.1:p.Arg435=
XM_005257583.3:c.949+1415C= (SGSH)	XP_005257640.1:n.949+1415C=
NM_000199.4:c.1305C= (SGSH)	NP_000190.1:p.Arg435=
NM_001352921.1:c.*392C= (SGSH)	NP_001339850.1:n.*392C=
NM_001352922.1:c.*355C= (SGSH)	NP_001339851.1:n.*355C=
NR_148201.1:n.1286C= (SGSH)
XM_005257583.4:c.949+1415C= (SGSH)	XP_005257640.1:n.949+1415C=
XM_017024952.1:c.*1209C= (SGSH)	XP_016880441.1:n.*1209C=
XR_001752585.1:n.1325C= (SGSH)
XR_001752586.1:n.969+1415C= (SGSH)
XR_001752587.1:n.969+1415C= (SGSH)
XR_001752588.1:n.969+1415C= (SGSH)
XR_001752589.1:n.969+1415C= (SGSH)
XR_001752590.1:n.969+1415C= (SGSH)
XR_001752591.1:n.969+1415C= (SGSH)
XR_001752592.1:n.969+1415C= (SGSH)
XR_002958057.1:n.1024+1213C= (SGSH)
NM_000199.5:c.1305C= (SGSH) MANE Select	NP_000190.1:p.Arg435=
NM_001352921.2:c.*392C= (SGSH)	NP_001339850.1:n.*392C=
NM_001352922.2:c.*355C= (SGSH)	NP_001339851.1:n.*355C=
NR_148201.2:n.1219C= (SGSH)
NM_001352921.3:c.*392C= (SGSH)	NP_001339850.1:n.*392C=