Canonical Allele Identifier: CA2277863848

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80213817G= , CM000679.2:g.80213817G=	GRCh38
NC_000017.10:g.78187616G= , CM000679.1:g.78187616G=	GRCh37
NC_000017.9:g.75802211G=	NCBI36
NG_008229.1:g.11584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-2049G= (CARD14)
ENST00000326317.11:c.732C= (SGSH) MANE Select	ENSP00000314606.6:p.Gly244=
ENST00000326317.10:c.732C= (SGSH)	ENSP00000314606.6:p.Gly244=
ENST00000570923.1:c.767C= (SGSH)	ENSP00000458200.1:p.Ala256=
ENST00000572257.5:c.334C= (SGSH)
ENST00000573150.5:c.626C= (SGSH)	ENSP00000459280.1:p.Ala209=
ENST00000575282.5:n.1027C= (SGSH)
ENST00000576941.5:c.*148C= (SGSH)	ENSP00000461160.1:n.*148C=
NM_000199.3:c.732C= (SGSH)	NP_000190.1:p.Gly244=
XM_005257582.2:c.732C= (SGSH)	XP_005257639.1:p.Gly244=
XM_005257583.3:c.732C= (SGSH)	XP_005257640.1:p.Gly244=
XM_011525126.1:c.732C= (SGSH)	XP_011523428.1:p.Gly244=
XM_011525127.1:c.732C= (SGSH)	XP_011523429.1:p.Gly244=
XR_934532.1:n.752C= (SGSH)
NM_000199.4:c.732C= (SGSH)	NP_000190.1:p.Gly244=
NM_001352921.1:c.732C= (SGSH)	NP_001339850.1:p.Gly244=
NM_001352922.1:c.732C= (SGSH)	NP_001339851.1:p.Gly244=
NR_148201.1:n.713C= (SGSH)
XM_005257583.4:c.732C= (SGSH)	XP_005257640.1:p.Gly244=
XM_017024952.1:c.732C= (SGSH)	XP_016880441.1:p.Gly244=
XR_001752585.1:n.752C= (SGSH)
XR_001752586.1:n.752C= (SGSH)
XR_001752587.1:n.752C= (SGSH)
XR_001752588.1:n.752C= (SGSH)
XR_001752589.1:n.752C= (SGSH)
XR_001752590.1:n.752C= (SGSH)
XR_001752591.1:n.752C= (SGSH)
XR_001752592.1:n.752C= (SGSH)
XR_002958057.1:n.752C= (SGSH)
XR_934532.2:n.752C= (SGSH)
NM_000199.5:c.732C= (SGSH) MANE Select	NP_000190.1:p.Gly244=
NM_001352921.2:c.732C= (SGSH)	NP_001339850.1:p.Gly244=
NM_001352922.2:c.732C= (SGSH)	NP_001339851.1:p.Gly244=
NR_148201.2:n.646C= (SGSH)
NM_001352921.3:c.732C= (SGSH)	NP_001339850.1:p.Gly244=