Canonical Allele Identifier: CA401362804

Gene: CARD14 SGSH

Linked Data

• ClinVar Variation Id: 958222
• ClinVar RCV Id: RCV001231341 ; RCV001760233
• dbSNP Id: rs1408975480
• gnomAD v2: 17-78188480-T-C
• gnomAD v3: 17-80214681-T-C
• gnomAD v4: 17-80214681-T-C
• COSMIC: COSM5741178
• MyVariant Identifiers: chr17:g.78188480T>C (hg19) ; chr17:g.80214681T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214681T>C , CM000679.2:g.80214681T>C	GRCh38
NC_000017.10:g.78188480T>C , CM000679.1:g.78188480T>C	GRCh37
NC_000017.9:g.75803075T>C	NCBI36
NG_008229.1:g.10720A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2845-1185T>C (CARD14)
ENST00000326317.11:c.440A>G (SGSH) MANE Select	ENSP00000314606.6:p.Gln147Arg
ENST00000326317.10:c.440A>G (SGSH)	ENSP00000314606.6:p.Gln147Arg
ENST00000570427.1:c.458A>G (SGSH)	ENSP00000459765.1:p.Gln153Arg
ENST00000570923.1:c.475A>G (SGSH)	ENSP00000458200.1:p.Arg159Gly
ENST00000571051.5:n.376-353A>G (SGSH)
ENST00000571675.5:n.460A>G (SGSH)
ENST00000572208.5:n.374-353A>G (SGSH)
ENST00000572257.5:c.42A>G (SGSH)
ENST00000573150.5:c.334A>G (SGSH)	ENSP00000459280.1:p.Arg112Gly
ENST00000574505.5:c.301-2A>G (SGSH)
ENST00000575282.5:n.449A>G (SGSH)
ENST00000576707.5:c.179A>G (SGSH)	ENSP00000461128.1:p.Gln60Arg
ENST00000576941.5:c.250-353A>G (SGSH)	ENSP00000461160.1:n.250-353A>G
NM_000199.3:c.440A>G (SGSH)	NP_000190.1:p.Gln147Arg
XM_005257582.2:c.440A>G (SGSH)	XP_005257639.1:p.Gln147Arg
XM_005257583.3:c.440A>G (SGSH)	XP_005257640.1:p.Gln147Arg
XM_011525126.1:c.440A>G (SGSH)	XP_011523428.1:p.Gln147Arg
XM_011525127.1:c.440A>G (SGSH)	XP_011523429.1:p.Gln147Arg
XR_934532.1:n.460A>G (SGSH)
NM_000199.4:c.440A>G (SGSH)	NP_000190.1:p.Gln147Arg
NM_001352921.1:c.440A>G (SGSH)	NP_001339850.1:p.Gln147Arg
NM_001352922.1:c.440A>G (SGSH)	NP_001339851.1:p.Gln147Arg
NR_148201.1:n.421A>G (SGSH)
XM_005257583.4:c.440A>G (SGSH)	XP_005257640.1:p.Gln147Arg
XM_017024952.1:c.440A>G (SGSH)	XP_016880441.1:p.Gln147Arg
XR_001752585.1:n.460A>G (SGSH)
XR_001752586.1:n.460A>G (SGSH)
XR_001752587.1:n.460A>G (SGSH)
XR_001752588.1:n.460A>G (SGSH)
XR_001752589.1:n.460A>G (SGSH)
XR_001752590.1:n.460A>G (SGSH)
XR_001752591.1:n.460A>G (SGSH)
XR_001752592.1:n.460A>G (SGSH)
XR_002958057.1:n.460A>G (SGSH)
XR_934532.2:n.460A>G (SGSH)
NM_000199.5:c.440A>G (SGSH) MANE Select	NP_000190.1:p.Gln147Arg
NM_001352921.2:c.440A>G (SGSH)	NP_001339850.1:p.Gln147Arg
NM_001352922.2:c.440A>G (SGSH)	NP_001339851.1:p.Gln147Arg
NR_148201.2:n.354A>G (SGSH)
NM_001352921.3:c.440A>G (SGSH)	NP_001339850.1:p.Gln147Arg