Canonical Allele Identifier: CA2277864316

Gene: CARD14 SGSH

Linked Data

• ClinVar Variation Id: 1373610
• ClinVar RCV Id: RCV001877396
• dbSNP Id: rs1460108613
• gnomAD v4: 17-80214612-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214612T>C , CM000679.2:g.80214612T>C	GRCh38
NC_000017.10:g.78188411T>C , CM000679.1:g.78188411T>C	GRCh37
NC_000017.9:g.75803006T>C	NCBI36
NG_008229.1:g.10789A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-1254T>C (CARD14)
ENST00000326317.11:c.506+3A>G (SGSH) MANE Select	ENSP00000314606.6:n.506+3A>G
ENST00000326317.10:c.506+3A>G (SGSH)	ENSP00000314606.6:n.506+3A>G
ENST00000570427.1:c.524+3A>G (SGSH)	ENSP00000459765.1:n.524+3A>G
ENST00000570923.1:c.541+3A>G (SGSH)	ENSP00000458200.1:n.541+3A>G
ENST00000571051.5:n.376-284A>G (SGSH)
ENST00000571675.5:n.529A>G (SGSH)
ENST00000572208.5:n.374-284A>G (SGSH)
ENST00000572257.5:c.108+3A>G (SGSH)
ENST00000573150.5:c.400+3A>G (SGSH)	ENSP00000459280.1:n.400+3A>G
ENST00000574505.5:c.365+3A>G (SGSH)
ENST00000575282.5:n.515+3A>G (SGSH)
ENST00000576707.5:c.245+3A>G (SGSH)	ENSP00000461128.1:n.245+3A>G
ENST00000576941.5:c.250-284A>G (SGSH)	ENSP00000461160.1:n.250-284A>G
NM_000199.3:c.506+3A>G (SGSH)	NP_000190.1:n.506+3A>G
XM_005257582.2:c.506+3A>G (SGSH)	XP_005257639.1:n.506+3A>G
XM_005257583.3:c.506+3A>G (SGSH)	XP_005257640.1:n.506+3A>G
XM_011525126.1:c.506+3A>G (SGSH)	XP_011523428.1:n.506+3A>G
XM_011525127.1:c.506+3A>G (SGSH)	XP_011523429.1:n.506+3A>G
XR_934532.1:n.526+3A>G (SGSH)
NM_000199.4:c.506+3A>G (SGSH)	NP_000190.1:n.506+3A>G
NM_001352921.1:c.506+3A>G (SGSH)	NP_001339850.1:n.506+3A>G
NM_001352922.1:c.506+3A>G (SGSH)	NP_001339851.1:n.506+3A>G
NR_148201.1:n.487+3A>G (SGSH)
XM_005257583.4:c.506+3A>G (SGSH)	XP_005257640.1:n.506+3A>G
XM_017024952.1:c.506+3A>G (SGSH)	XP_016880441.1:n.506+3A>G
XR_001752585.1:n.526+3A>G (SGSH)
XR_001752586.1:n.526+3A>G (SGSH)
XR_001752587.1:n.526+3A>G (SGSH)
XR_001752588.1:n.526+3A>G (SGSH)
XR_001752589.1:n.526+3A>G (SGSH)
XR_001752590.1:n.526+3A>G (SGSH)
XR_001752591.1:n.526+3A>G (SGSH)
XR_001752592.1:n.526+3A>G (SGSH)
XR_002958057.1:n.526+3A>G (SGSH)
XR_934532.2:n.526+3A>G (SGSH)
NM_000199.5:c.506+3A>G (SGSH) MANE Select	NP_000190.1:n.506+3A>G
NM_001352921.2:c.506+3A>G (SGSH)	NP_001339850.1:n.506+3A>G
NM_001352922.2:c.506+3A>G (SGSH)	NP_001339851.1:n.506+3A>G
NR_148201.2:n.420+3A>G (SGSH)
NM_001352921.3:c.506+3A>G (SGSH)	NP_001339850.1:n.506+3A>G