Canonical Allele Identifier: CA234924

Gene: CARD14 SGSH

Linked Data

• ClinVar Variation Id: 167682
• ClinVar RCV Id: RCV000153945 ; RCV001800465
• dbSNP Id: rs386799751
• MyVariant Identifiers: chr17:g.78187720_78187723delinsGC (hg19) ; chr17:g.80213921_80213924delinsGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80213921_80213924delinsGC , CM000679.2:g.80213921_80213924delinsGC	GRCh38
NC_000017.10:g.78187720_78187723delinsGC , CM000679.1:g.78187720_78187723delinsGC	GRCh37
NC_000017.9:g.75802315_75802318delinsGC	NCBI36
NG_008229.1:g.11477_11480delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2845-1945_2845-1942delinsGC (CARD14)
ENST00000326317.11:c.664-39_664-36delinsGC (SGSH) MANE Select	ENSP00000314606.6:n.664-39_664-36delinsGC
ENST00000326317.10:c.664-39_664-36delinsGC (SGSH)	ENSP00000314606.6:n.664-39_664-36delinsGC
ENST00000570923.1:c.699-39_699-36delinsGC (SGSH)	ENSP00000458200.1:n.699-39_699-36delinsGC
ENST00000572208.5:n.531-39_531-36delinsGC (SGSH)
ENST00000572257.5:c.266-39_266-36delinsGC (SGSH)
ENST00000573150.5:c.558-39_558-36delinsGC (SGSH)	ENSP00000459280.1:n.558-39_558-36delinsGC
ENST00000574505.5:c.523-39_523-36delinsGC (SGSH)
ENST00000575282.5:n.920_923delinsGC (SGSH)
ENST00000576941.5:c.*80-39_*80-36delinsGC (SGSH)	ENSP00000461160.1:n.*80-39_*80-36delinsGC
NM_000199.3:c.664-39_664-36delinsGC (SGSH)	NP_000190.1:n.664-39_664-36delinsGC
XM_005257582.2:c.664-39_664-36delinsGC (SGSH)	XP_005257639.1:n.664-39_664-36delinsGC
XM_005257583.3:c.664-39_664-36delinsGC (SGSH)	XP_005257640.1:n.664-39_664-36delinsGC
XM_011525126.1:c.664-39_664-36delinsGC (SGSH)	XP_011523428.1:n.664-39_664-36delinsGC
XM_011525127.1:c.664-39_664-36delinsGC (SGSH)	XP_011523429.1:n.664-39_664-36delinsGC
XR_934532.1:n.684-39_684-36delinsGC (SGSH)
NM_000199.4:c.664-39_664-36delinsGC (SGSH)	NP_000190.1:n.664-39_664-36delinsGC
NM_001352921.1:c.664-39_664-36delinsGC (SGSH)	NP_001339850.1:n.664-39_664-36delinsGC
NM_001352922.1:c.664-39_664-36delinsGC (SGSH)	NP_001339851.1:n.664-39_664-36delinsGC
NR_148201.1:n.645-39_645-36delinsGC (SGSH)
XM_005257583.4:c.664-39_664-36delinsGC (SGSH)	XP_005257640.1:n.664-39_664-36delinsGC
XM_017024952.1:c.664-39_664-36delinsGC (SGSH)	XP_016880441.1:n.664-39_664-36delinsGC
XR_001752585.1:n.684-39_684-36delinsGC (SGSH)
XR_001752586.1:n.684-39_684-36delinsGC (SGSH)
XR_001752587.1:n.684-39_684-36delinsGC (SGSH)
XR_001752588.1:n.684-39_684-36delinsGC (SGSH)
XR_001752589.1:n.684-39_684-36delinsGC (SGSH)
XR_001752590.1:n.684-39_684-36delinsGC (SGSH)
XR_001752591.1:n.684-39_684-36delinsGC (SGSH)
XR_001752592.1:n.684-39_684-36delinsGC (SGSH)
XR_002958057.1:n.684-39_684-36delinsGC (SGSH)
XR_934532.2:n.684-39_684-36delinsGC (SGSH)
NM_000199.5:c.664-39_664-36delinsGC (SGSH) MANE Select	NP_000190.1:n.664-39_664-36delinsGC
NM_001352921.2:c.664-39_664-36delinsGC (SGSH)	NP_001339850.1:n.664-39_664-36delinsGC
NM_001352922.2:c.664-39_664-36delinsGC (SGSH)	NP_001339851.1:n.664-39_664-36delinsGC
NR_148201.2:n.578-39_578-36delinsGC (SGSH)
NM_001352921.3:c.664-39_664-36delinsGC (SGSH)	NP_001339850.1:n.664-39_664-36delinsGC