Canonical Allele Identifier: CA2573155032

Gene: CARD14 SGSH

Linked Data

• ClinVar Variation Id: 1570684
• ClinVar RCV Id: RCV002215557
• dbSNP Id: rs2144748073

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214608C>A , CM000679.2:g.80214608C>A	GRCh38
NC_000017.10:g.78188407C>A , CM000679.1:g.78188407C>A	GRCh37
NC_000017.9:g.75803002C>A	NCBI36
NG_008229.1:g.10793G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-1258C>A (CARD14)
ENST00000326317.11:c.506+7G>T (SGSH) MANE Select	ENSP00000314606.6:n.506+7G>T
ENST00000326317.10:c.506+7G>T (SGSH)	ENSP00000314606.6:n.506+7G>T
ENST00000570427.1:c.524+7G>T (SGSH)	ENSP00000459765.1:n.524+7G>T
ENST00000570923.1:c.541+7G>T (SGSH)	ENSP00000458200.1:n.541+7G>T
ENST00000571051.5:n.376-280G>T (SGSH)
ENST00000571675.5:n.533G>T (SGSH)
ENST00000572208.5:n.374-280G>T (SGSH)
ENST00000572257.5:c.108+7G>T (SGSH)
ENST00000573150.5:c.400+7G>T (SGSH)	ENSP00000459280.1:n.400+7G>T
ENST00000574505.5:c.365+7G>T (SGSH)
ENST00000575282.5:n.515+7G>T (SGSH)
ENST00000576707.5:c.245+7G>T (SGSH)	ENSP00000461128.1:n.245+7G>T
ENST00000576941.5:c.250-280G>T (SGSH)	ENSP00000461160.1:n.250-280G>T
NM_000199.3:c.506+7G>T (SGSH)	NP_000190.1:n.506+7G>T
XM_005257582.2:c.506+7G>T (SGSH)	XP_005257639.1:n.506+7G>T
XM_005257583.3:c.506+7G>T (SGSH)	XP_005257640.1:n.506+7G>T
XM_011525126.1:c.506+7G>T (SGSH)	XP_011523428.1:n.506+7G>T
XM_011525127.1:c.506+7G>T (SGSH)	XP_011523429.1:n.506+7G>T
XR_934532.1:n.526+7G>T (SGSH)
NM_000199.4:c.506+7G>T (SGSH)	NP_000190.1:n.506+7G>T
NM_001352921.1:c.506+7G>T (SGSH)	NP_001339850.1:n.506+7G>T
NM_001352922.1:c.506+7G>T (SGSH)	NP_001339851.1:n.506+7G>T
NR_148201.1:n.487+7G>T (SGSH)
XM_005257583.4:c.506+7G>T (SGSH)	XP_005257640.1:n.506+7G>T
XM_017024952.1:c.506+7G>T (SGSH)	XP_016880441.1:n.506+7G>T
XR_001752585.1:n.526+7G>T (SGSH)
XR_001752586.1:n.526+7G>T (SGSH)
XR_001752587.1:n.526+7G>T (SGSH)
XR_001752588.1:n.526+7G>T (SGSH)
XR_001752589.1:n.526+7G>T (SGSH)
XR_001752590.1:n.526+7G>T (SGSH)
XR_001752591.1:n.526+7G>T (SGSH)
XR_001752592.1:n.526+7G>T (SGSH)
XR_002958057.1:n.526+7G>T (SGSH)
XR_934532.2:n.526+7G>T (SGSH)
NM_000199.5:c.506+7G>T (SGSH) MANE Select	NP_000190.1:n.506+7G>T
NM_001352921.2:c.506+7G>T (SGSH)	NP_001339850.1:n.506+7G>T
NM_001352922.2:c.506+7G>T (SGSH)	NP_001339851.1:n.506+7G>T
NR_148201.2:n.420+7G>T (SGSH)
NM_001352921.3:c.506+7G>T (SGSH)	NP_001339850.1:n.506+7G>T