Canonical Allele Identifier: CA2277863863

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80213838G= , CM000679.2:g.80213838G=	GRCh38
NC_000017.10:g.78187637G= , CM000679.1:g.78187637G=	GRCh37
NC_000017.9:g.75802232G=	NCBI36
NG_008229.1:g.11563C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-2028G= (CARD14)
ENST00000326317.11:c.711C= (SGSH) MANE Select	ENSP00000314606.6:p.Ala237=
ENST00000326317.10:c.711C= (SGSH)	ENSP00000314606.6:p.Ala237=
ENST00000570923.1:c.746C= (SGSH)	ENSP00000458200.1:p.Pro249=
ENST00000572208.5:n.578C= (SGSH)
ENST00000572257.5:c.313C= (SGSH)
ENST00000573150.5:c.605C= (SGSH)	ENSP00000459280.1:p.Pro202=
ENST00000574505.5:c.570C= (SGSH)
ENST00000575282.5:n.1006C= (SGSH)
ENST00000576941.5:c.*127C= (SGSH)	ENSP00000461160.1:n.*127C=
NM_000199.3:c.711C= (SGSH)	NP_000190.1:p.Ala237=
XM_005257582.2:c.711C= (SGSH)	XP_005257639.1:p.Ala237=
XM_005257583.3:c.711C= (SGSH)	XP_005257640.1:p.Ala237=
XM_011525126.1:c.711C= (SGSH)	XP_011523428.1:p.Ala237=
XM_011525127.1:c.711C= (SGSH)	XP_011523429.1:p.Ala237=
XR_934532.1:n.731C= (SGSH)
NM_000199.4:c.711C= (SGSH)	NP_000190.1:p.Ala237=
NM_001352921.1:c.711C= (SGSH)	NP_001339850.1:p.Ala237=
NM_001352922.1:c.711C= (SGSH)	NP_001339851.1:p.Ala237=
NR_148201.1:n.692C= (SGSH)
XM_005257583.4:c.711C= (SGSH)	XP_005257640.1:p.Ala237=
XM_017024952.1:c.711C= (SGSH)	XP_016880441.1:p.Ala237=
XR_001752585.1:n.731C= (SGSH)
XR_001752586.1:n.731C= (SGSH)
XR_001752587.1:n.731C= (SGSH)
XR_001752588.1:n.731C= (SGSH)
XR_001752589.1:n.731C= (SGSH)
XR_001752590.1:n.731C= (SGSH)
XR_001752591.1:n.731C= (SGSH)
XR_001752592.1:n.731C= (SGSH)
XR_002958057.1:n.731C= (SGSH)
XR_934532.2:n.731C= (SGSH)
NM_000199.5:c.711C= (SGSH) MANE Select	NP_000190.1:p.Ala237=
NM_001352921.2:c.711C= (SGSH)	NP_001339850.1:p.Ala237=
NM_001352922.2:c.711C= (SGSH)	NP_001339851.1:p.Ala237=
NR_148201.2:n.625C= (SGSH)
NM_001352921.3:c.711C= (SGSH)	NP_001339850.1:p.Ala237=