Canonical Allele Identifier: CA2277864286

Gene: CARD14 SGSH

Linked Data

• dbSNP Id: rs1567923031
• gnomAD v4: 17-80214579-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214579C>T , CM000679.2:g.80214579C>T	GRCh38
NC_000017.10:g.78188378C>T , CM000679.1:g.78188378C>T	GRCh37
NC_000017.9:g.75802973C>T	NCBI36
NG_008229.1:g.10822G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2845-1287C>T (CARD14)
ENST00000326317.11:c.506+36G>A (SGSH) MANE Select	ENSP00000314606.6:n.506+36G>A
ENST00000326317.10:c.506+36G>A (SGSH)	ENSP00000314606.6:n.506+36G>A
ENST00000570427.1:c.524+36G>A (SGSH)	ENSP00000459765.1:n.524+36G>A
ENST00000570923.1:c.541+36G>A (SGSH)	ENSP00000458200.1:n.541+36G>A
ENST00000571051.5:n.376-251G>A (SGSH)
ENST00000571675.5:n.562G>A (SGSH)
ENST00000572208.5:n.374-251G>A (SGSH)
ENST00000572257.5:c.108+36G>A (SGSH)
ENST00000573150.5:c.400+36G>A (SGSH)	ENSP00000459280.1:n.400+36G>A
ENST00000574505.5:c.365+36G>A (SGSH)
ENST00000575282.5:n.515+36G>A (SGSH)
ENST00000576707.5:c.245+36G>A (SGSH)	ENSP00000461128.1:n.245+36G>A
ENST00000576941.5:c.250-251G>A (SGSH)	ENSP00000461160.1:n.250-251G>A
NM_000199.3:c.506+36G>A (SGSH)	NP_000190.1:n.506+36G>A
XM_005257582.2:c.506+36G>A (SGSH)	XP_005257639.1:n.506+36G>A
XM_005257583.3:c.506+36G>A (SGSH)	XP_005257640.1:n.506+36G>A
XM_011525126.1:c.506+36G>A (SGSH)	XP_011523428.1:n.506+36G>A
XM_011525127.1:c.506+36G>A (SGSH)	XP_011523429.1:n.506+36G>A
XR_934532.1:n.526+36G>A (SGSH)
NM_000199.4:c.506+36G>A (SGSH)	NP_000190.1:n.506+36G>A
NM_001352921.1:c.506+36G>A (SGSH)	NP_001339850.1:n.506+36G>A
NM_001352922.1:c.506+36G>A (SGSH)	NP_001339851.1:n.506+36G>A
NR_148201.1:n.487+36G>A (SGSH)
XM_005257583.4:c.506+36G>A (SGSH)	XP_005257640.1:n.506+36G>A
XM_017024952.1:c.506+36G>A (SGSH)	XP_016880441.1:n.506+36G>A
XR_001752585.1:n.526+36G>A (SGSH)
XR_001752586.1:n.526+36G>A (SGSH)
XR_001752587.1:n.526+36G>A (SGSH)
XR_001752588.1:n.526+36G>A (SGSH)
XR_001752589.1:n.526+36G>A (SGSH)
XR_001752590.1:n.526+36G>A (SGSH)
XR_001752591.1:n.526+36G>A (SGSH)
XR_001752592.1:n.526+36G>A (SGSH)
XR_002958057.1:n.526+36G>A (SGSH)
XR_934532.2:n.526+36G>A (SGSH)
NM_000199.5:c.506+36G>A (SGSH) MANE Select	NP_000190.1:n.506+36G>A
NM_001352921.2:c.506+36G>A (SGSH)	NP_001339850.1:n.506+36G>A
NM_001352922.2:c.506+36G>A (SGSH)	NP_001339851.1:n.506+36G>A
NR_148201.2:n.420+36G>A (SGSH)
NM_001352921.3:c.506+36G>A (SGSH)	NP_001339850.1:n.506+36G>A