Canonical Allele Identifier: CA2277862154

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210430G= , CM000679.2:g.80210430G=	GRCh38
NC_000017.10:g.78184229G= , CM000679.1:g.78184229G=	GRCh37
NC_000017.9:g.75798824G=	NCBI36
NG_008229.1:g.14971C=
NG_032778.1:g.45439G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2844+1172G= (CARD14)
ENST00000326317.11:c.*22C= (SGSH) MANE Select	ENSP00000314606.6:n.*22C=
ENST00000326317.10:c.*22C= (SGSH)	ENSP00000314606.6:n.*22C=
ENST00000572257.5:c.551+1641C= (SGSH)
ENST00000573150.5:c.*741C= (SGSH)	ENSP00000459280.1:n.*741C=
ENST00000575282.5:n.4414C= (SGSH)
ENST00000576856.1:c.785C= (SGSH)	ENSP00000460720.1:n.785C=
NM_000199.3:c.*22C= (SGSH)	NP_000190.1:n.*22C=
XM_005257583.3:c.949+1641C= (SGSH)	XP_005257640.1:n.949+1641C=
NM_000199.4:c.*22C= (SGSH)	NP_000190.1:n.*22C=
NM_001352921.1:c.*618C= (SGSH)	NP_001339850.1:n.*618C=
NM_001352922.1:c.*581C= (SGSH)	NP_001339851.1:n.*581C=
NR_148201.1:n.1512C= (SGSH)
XM_005257583.4:c.949+1641C= (SGSH)	XP_005257640.1:n.949+1641C=
XM_017024952.1:c.*1435C= (SGSH)	XP_016880441.1:n.*1435C=
XR_001752585.1:n.1551C= (SGSH)
XR_001752586.1:n.969+1641C= (SGSH)
XR_001752587.1:n.969+1641C= (SGSH)
XR_001752588.1:n.969+1641C= (SGSH)
XR_001752589.1:n.969+1641C= (SGSH)
XR_001752590.1:n.969+1641C= (SGSH)
XR_001752591.1:n.969+1641C= (SGSH)
XR_001752592.1:n.969+1641C= (SGSH)
XR_002958057.1:n.1024+1439C= (SGSH)
NM_000199.5:c.*22C= (SGSH) MANE Select	NP_000190.1:n.*22C=
NM_001352921.2:c.*618C= (SGSH)	NP_001339850.1:n.*618C=
NM_001352922.2:c.*581C= (SGSH)	NP_001339851.1:n.*581C=
NR_148201.2:n.1445C= (SGSH)
NM_001352921.3:c.*618C= (SGSH)	NP_001339850.1:n.*618C=