Canonical Allele Identifier: CA2277862968

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80212045C= , CM000679.2:g.80212045C=	GRCh38
NC_000017.10:g.78185844C= , CM000679.1:g.78185844C=	GRCh37
NC_000017.9:g.75800439C=	NCBI36
NG_008229.1:g.13356G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2844+2787C= (CARD14)
ENST00000326317.11:c.949+26G= (SGSH) MANE Select	ENSP00000314606.6:n.949+26G=
ENST00000326317.10:c.949+26G= (SGSH)	ENSP00000314606.6:n.949+26G=
ENST00000570923.1:c.*185G= (SGSH)	ENSP00000458200.1:n.*185G=
ENST00000572257.5:c.551+26G= (SGSH)
ENST00000573150.5:c.*159+26G= (SGSH)	ENSP00000459280.1:n.*159+26G=
ENST00000575282.5:n.2799G= (SGSH)
ENST00000576856.1:c.148+26G= (SGSH)	ENSP00000460720.1:n.148+26G=
NM_000199.3:c.949+26G= (SGSH)	NP_000190.1:n.949+26G=
XM_005257582.2:c.949+26G= (SGSH)	XP_005257639.1:n.949+26G=
XM_005257583.3:c.949+26G= (SGSH)	XP_005257640.1:n.949+26G=
XM_011525126.1:c.949+26G= (SGSH)	XP_011523428.1:n.949+26G=
XM_011525127.1:c.949+26G= (SGSH)	XP_011523429.1:n.949+26G=
XR_934532.1:n.995G= (SGSH)
NM_000199.4:c.949+26G= (SGSH)	NP_000190.1:n.949+26G=
NM_001352921.1:c.949+26G= (SGSH)	NP_001339850.1:n.949+26G=
NM_001352922.1:c.949+26G= (SGSH)	NP_001339851.1:n.949+26G=
NR_148201.1:n.930+26G= (SGSH)
XM_005257583.4:c.949+26G= (SGSH)	XP_005257640.1:n.949+26G=
XM_017024952.1:c.949+26G= (SGSH)	XP_016880441.1:n.949+26G=
XR_001752585.1:n.969+26G= (SGSH)
XR_001752586.1:n.969+26G= (SGSH)
XR_001752587.1:n.969+26G= (SGSH)
XR_001752588.1:n.969+26G= (SGSH)
XR_001752589.1:n.969+26G= (SGSH)
XR_001752590.1:n.969+26G= (SGSH)
XR_001752591.1:n.969+26G= (SGSH)
XR_001752592.1:n.969+26G= (SGSH)
XR_002958057.1:n.969+26G= (SGSH)
XR_934532.2:n.995G= (SGSH)
NM_000199.5:c.949+26G= (SGSH) MANE Select	NP_000190.1:n.949+26G=
NM_001352921.2:c.949+26G= (SGSH)	NP_001339850.1:n.949+26G=
NM_001352922.2:c.949+26G= (SGSH)	NP_001339851.1:n.949+26G=
NR_148201.2:n.863+26G= (SGSH)
NM_001352921.3:c.949+26G= (SGSH)	NP_001339850.1:n.949+26G=