Canonical Allele Identifier: CA2277864116

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214264C= , CM000679.2:g.80214264C=	GRCh38
NC_000017.10:g.78188063C= , CM000679.1:g.78188063C=	GRCh37
NC_000017.9:g.75802658C=	NCBI36
NG_008229.1:g.11137G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-1602C= (CARD14)
ENST00000326317.11:c.571G= (SGSH) MANE Select	ENSP00000314606.6:p.Gly191=
ENST00000326317.10:c.571G= (SGSH)	ENSP00000314606.6:p.Gly191=
ENST00000570923.1:c.606G= (SGSH)	ENSP00000458200.1:p.Thr202=
ENST00000571051.5:n.440G= (SGSH)
ENST00000572208.5:n.438G= (SGSH)
ENST00000572257.5:c.173G= (SGSH)
ENST00000573150.5:c.465G= (SGSH)	ENSP00000459280.1:p.Thr155=
ENST00000574505.5:c.430G= (SGSH)
ENST00000575282.5:n.580G= (SGSH)
ENST00000576707.5:c.310G= (SGSH)	ENSP00000461128.1:p.Gly104=
ENST00000576941.5:c.314G= (SGSH)	ENSP00000461160.1:p.Arg105=
NM_000199.3:c.571G= (SGSH)	NP_000190.1:p.Gly191=
XM_005257582.2:c.571G= (SGSH)	XP_005257639.1:p.Gly191=
XM_005257583.3:c.571G= (SGSH)	XP_005257640.1:p.Gly191=
XM_011525126.1:c.571G= (SGSH)	XP_011523428.1:p.Gly191=
XM_011525127.1:c.571G= (SGSH)	XP_011523429.1:p.Gly191=
XR_934532.1:n.591G= (SGSH)
NM_000199.4:c.571G= (SGSH)	NP_000190.1:p.Gly191=
NM_001352921.1:c.571G= (SGSH)	NP_001339850.1:p.Gly191=
NM_001352922.1:c.571G= (SGSH)	NP_001339851.1:p.Gly191=
NR_148201.1:n.552G= (SGSH)
XM_005257583.4:c.571G= (SGSH)	XP_005257640.1:p.Gly191=
XM_017024952.1:c.571G= (SGSH)	XP_016880441.1:p.Gly191=
XR_001752585.1:n.591G= (SGSH)
XR_001752586.1:n.591G= (SGSH)
XR_001752587.1:n.591G= (SGSH)
XR_001752588.1:n.591G= (SGSH)
XR_001752589.1:n.591G= (SGSH)
XR_001752590.1:n.591G= (SGSH)
XR_001752591.1:n.591G= (SGSH)
XR_001752592.1:n.591G= (SGSH)
XR_002958057.1:n.591G= (SGSH)
XR_934532.2:n.591G= (SGSH)
NM_000199.5:c.571G= (SGSH) MANE Select	NP_000190.1:p.Gly191=
NM_001352921.2:c.571G= (SGSH)	NP_001339850.1:p.Gly191=
NM_001352922.2:c.571G= (SGSH)	NP_001339851.1:p.Gly191=
NR_148201.2:n.485G= (SGSH)
NM_001352921.3:c.571G= (SGSH)	NP_001339850.1:p.Gly191=