Canonical Allele Identifier: CA2277862366

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210826C= , CM000679.2:g.80210826C=	GRCh38
NC_000017.10:g.78184625C= , CM000679.1:g.78184625C=	GRCh37
NC_000017.9:g.75799220C=	NCBI36
NG_008229.1:g.14575G=
NG_032778.1:g.45835C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1568C= (CARD14)
ENST00000326317.11:c.1135G= (SGSH) MANE Select	ENSP00000314606.6:p.Val379=
ENST00000326317.10:c.1135G= (SGSH)	ENSP00000314606.6:p.Val379=
ENST00000572257.5:c.551+1245G= (SGSH)
ENST00000573150.5:c.*345G= (SGSH)	ENSP00000459280.1:n.*345G=
ENST00000575282.5:n.4018G= (SGSH)
ENST00000576856.1:c.389G= (SGSH)	ENSP00000460720.1:n.389G=
NM_000199.3:c.1135G= (SGSH)	NP_000190.1:p.Val379=
XM_005257583.3:c.949+1245G= (SGSH)	XP_005257640.1:n.949+1245G=
NM_000199.4:c.1135G= (SGSH)	NP_000190.1:p.Val379=
NM_001352921.1:c.*222G= (SGSH)	NP_001339850.1:n.*222G=
NM_001352922.1:c.*185G= (SGSH)	NP_001339851.1:n.*185G=
NR_148201.1:n.1116G= (SGSH)
XM_005257583.4:c.949+1245G= (SGSH)	XP_005257640.1:n.949+1245G=
XM_017024952.1:c.*1039G= (SGSH)	XP_016880441.1:n.*1039G=
XR_001752585.1:n.1155G= (SGSH)
XR_001752586.1:n.969+1245G= (SGSH)
XR_001752587.1:n.969+1245G= (SGSH)
XR_001752588.1:n.969+1245G= (SGSH)
XR_001752589.1:n.969+1245G= (SGSH)
XR_001752590.1:n.969+1245G= (SGSH)
XR_001752591.1:n.969+1245G= (SGSH)
XR_001752592.1:n.969+1245G= (SGSH)
XR_002958057.1:n.1024+1043G= (SGSH)
NM_000199.5:c.1135G= (SGSH) MANE Select	NP_000190.1:p.Val379=
NM_001352921.2:c.*222G= (SGSH)	NP_001339850.1:n.*222G=
NM_001352922.2:c.*185G= (SGSH)	NP_001339851.1:n.*185G=
NR_148201.2:n.1049G= (SGSH)
NM_001352921.3:c.*222G= (SGSH)	NP_001339850.1:n.*222G=