Canonical Allele Identifier: CA2277862212

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210527G= , CM000679.2:g.80210527G=	GRCh38
NC_000017.10:g.78184326G= , CM000679.1:g.78184326G=	GRCh37
NC_000017.9:g.75798921G=	NCBI36
NG_008229.1:g.14874C=
NG_032778.1:g.45536G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2844+1269G= (CARD14)
ENST00000326317.11:c.1434C= (SGSH) MANE Select	ENSP00000314606.6:p.Pro478=
ENST00000326317.10:c.1434C= (SGSH)	ENSP00000314606.6:p.Pro478=
ENST00000572257.5:c.551+1544C= (SGSH)
ENST00000573150.5:c.*644C= (SGSH)	ENSP00000459280.1:n.*644C=
ENST00000575282.5:n.4317C= (SGSH)
ENST00000576856.1:c.688C= (SGSH)	ENSP00000460720.1:n.688C=
NM_000199.3:c.1434C= (SGSH)	NP_000190.1:p.Pro478=
XM_005257583.3:c.949+1544C= (SGSH)	XP_005257640.1:n.949+1544C=
NM_000199.4:c.1434C= (SGSH)	NP_000190.1:p.Pro478=
NM_001352921.1:c.*521C= (SGSH)	NP_001339850.1:n.*521C=
NM_001352922.1:c.*484C= (SGSH)	NP_001339851.1:n.*484C=
NR_148201.1:n.1415C= (SGSH)
XM_005257583.4:c.949+1544C= (SGSH)	XP_005257640.1:n.949+1544C=
XM_017024952.1:c.*1338C= (SGSH)	XP_016880441.1:n.*1338C=
XR_001752585.1:n.1454C= (SGSH)
XR_001752586.1:n.969+1544C= (SGSH)
XR_001752587.1:n.969+1544C= (SGSH)
XR_001752588.1:n.969+1544C= (SGSH)
XR_001752589.1:n.969+1544C= (SGSH)
XR_001752590.1:n.969+1544C= (SGSH)
XR_001752591.1:n.969+1544C= (SGSH)
XR_001752592.1:n.969+1544C= (SGSH)
XR_002958057.1:n.1024+1342C= (SGSH)
NM_000199.5:c.1434C= (SGSH) MANE Select	NP_000190.1:p.Pro478=
NM_001352921.2:c.*521C= (SGSH)	NP_001339850.1:n.*521C=
NM_001352922.2:c.*484C= (SGSH)	NP_001339851.1:n.*484C=
NR_148201.2:n.1348C= (SGSH)
NM_001352921.3:c.*521C= (SGSH)	NP_001339850.1:n.*521C=