Canonical Allele Identifier: CA2277862094

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210331T= , CM000679.2:g.80210331T=	GRCh38
NC_000017.10:g.78184130T= , CM000679.1:g.78184130T=	GRCh37
NC_000017.9:g.75798725T=	NCBI36
NG_008229.1:g.15070A=
NG_032778.1:g.45340T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1073T= (CARD14)
ENST00000326317.11:c.*121A= (SGSH) MANE Select	ENSP00000314606.6:n.*121A=
ENST00000326317.10:c.*121A= (SGSH)	ENSP00000314606.6:n.*121A=
ENST00000572257.5:c.551+1740A= (SGSH)
ENST00000573150.5:c.*840A= (SGSH)	ENSP00000459280.1:n.*840A=
ENST00000575282.5:n.4513A= (SGSH)
NM_000199.3:c.*121A= (SGSH)	NP_000190.1:n.*121A=
XM_005257583.3:c.949+1740A= (SGSH)	XP_005257640.1:n.949+1740A=
NM_000199.4:c.*121A= (SGSH)	NP_000190.1:n.*121A=
NM_001352921.1:c.*717A= (SGSH)	NP_001339850.1:n.*717A=
NM_001352922.1:c.*680A= (SGSH)	NP_001339851.1:n.*680A=
NR_148201.1:n.1611A= (SGSH)
XM_005257583.4:c.949+1740A= (SGSH)	XP_005257640.1:n.949+1740A=
XM_017024952.1:c.*1534A= (SGSH)	XP_016880441.1:n.*1534A=
XR_001752585.1:n.1650A= (SGSH)
XR_001752586.1:n.969+1740A= (SGSH)
XR_001752587.1:n.969+1740A= (SGSH)
XR_001752588.1:n.969+1740A= (SGSH)
XR_001752589.1:n.969+1740A= (SGSH)
XR_001752590.1:n.969+1740A= (SGSH)
XR_001752591.1:n.969+1740A= (SGSH)
XR_001752592.1:n.969+1740A= (SGSH)
XR_002958057.1:n.1024+1538A= (SGSH)
NM_000199.5:c.*121A= (SGSH) MANE Select	NP_000190.1:n.*121A=
NM_001352921.2:c.*717A= (SGSH)	NP_001339850.1:n.*717A=
NM_001352922.2:c.*680A= (SGSH)	NP_001339851.1:n.*680A=
NR_148201.2:n.1544A= (SGSH)
NM_001352921.3:c.*717A= (SGSH)	NP_001339850.1:n.*717A=