Canonical Allele Identifier: CA2277862333

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210767G= , CM000679.2:g.80210767G=	GRCh38
NC_000017.10:g.78184566G= , CM000679.1:g.78184566G=	GRCh37
NC_000017.9:g.75799161G=	NCBI36
NG_008229.1:g.14634C=
NG_032778.1:g.45776G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2844+1509G= (CARD14)
ENST00000326317.11:c.1194C= (SGSH) MANE Select	ENSP00000314606.6:p.Ile398=
ENST00000326317.10:c.1194C= (SGSH)	ENSP00000314606.6:p.Ile398=
ENST00000572257.5:c.551+1304C= (SGSH)
ENST00000573150.5:c.*404C= (SGSH)	ENSP00000459280.1:n.*404C=
ENST00000575282.5:n.4077C= (SGSH)
ENST00000576856.1:c.448C= (SGSH)	ENSP00000460720.1:n.448C=
NM_000199.3:c.1194C= (SGSH)	NP_000190.1:p.Ile398=
XM_005257583.3:c.949+1304C= (SGSH)	XP_005257640.1:n.949+1304C=
NM_000199.4:c.1194C= (SGSH)	NP_000190.1:p.Ile398=
NM_001352921.1:c.*281C= (SGSH)	NP_001339850.1:n.*281C=
NM_001352922.1:c.*244C= (SGSH)	NP_001339851.1:n.*244C=
NR_148201.1:n.1175C= (SGSH)
XM_005257583.4:c.949+1304C= (SGSH)	XP_005257640.1:n.949+1304C=
XM_017024952.1:c.*1098C= (SGSH)	XP_016880441.1:n.*1098C=
XR_001752585.1:n.1214C= (SGSH)
XR_001752586.1:n.969+1304C= (SGSH)
XR_001752587.1:n.969+1304C= (SGSH)
XR_001752588.1:n.969+1304C= (SGSH)
XR_001752589.1:n.969+1304C= (SGSH)
XR_001752590.1:n.969+1304C= (SGSH)
XR_001752591.1:n.969+1304C= (SGSH)
XR_001752592.1:n.969+1304C= (SGSH)
XR_002958057.1:n.1024+1102C= (SGSH)
NM_000199.5:c.1194C= (SGSH) MANE Select	NP_000190.1:p.Ile398=
NM_001352921.2:c.*281C= (SGSH)	NP_001339850.1:n.*281C=
NM_001352922.2:c.*244C= (SGSH)	NP_001339851.1:n.*244C=
NR_148201.2:n.1108C= (SGSH)
NM_001352921.3:c.*281C= (SGSH)	NP_001339850.1:n.*281C=