Canonical Allele Identifier: CA2640319533

Gene: CARD14 SGSH

Linked Data

• gnomAD v4: 17-80210276-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210276C>G , CM000679.2:g.80210276C>G	GRCh38
NC_000017.10:g.78184075C>G , CM000679.1:g.78184075C>G	GRCh37
NC_000017.9:g.75798670C>G	NCBI36
NG_008229.1:g.15125G>C
NG_032778.1:g.45285C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1018C>G (CARD14)
ENST00000326317.11:c.*176G>C (SGSH) MANE Select	ENSP00000314606.6:n.*176G>C
ENST00000326317.10:c.*176G>C (SGSH)	ENSP00000314606.6:n.*176G>C
ENST00000572257.5:c.551+1795G>C (SGSH)
ENST00000573150.5:c.*895G>C (SGSH)	ENSP00000459280.1:n.*895G>C
ENST00000575282.5:n.4568G>C (SGSH)
NM_000199.3:c.*176G>C (SGSH)	NP_000190.1:n.*176G>C
XM_005257583.3:c.949+1795G>C (SGSH)	XP_005257640.1:n.949+1795G>C
NM_000199.4:c.*176G>C (SGSH)	NP_000190.1:n.*176G>C
NM_001352921.1:c.*772G>C (SGSH)	NP_001339850.1:n.*772G>C
NM_001352922.1:c.*735G>C (SGSH)	NP_001339851.1:n.*735G>C
NR_148201.1:n.1666G>C (SGSH)
XM_005257583.4:c.949+1795G>C (SGSH)	XP_005257640.1:n.949+1795G>C
XM_017024952.1:c.*1589G>C (SGSH)	XP_016880441.1:n.*1589G>C
XR_001752585.1:n.1705G>C (SGSH)
XR_001752586.1:n.969+1795G>C (SGSH)
XR_001752587.1:n.969+1795G>C (SGSH)
XR_001752588.1:n.969+1795G>C (SGSH)
XR_001752589.1:n.969+1795G>C (SGSH)
XR_001752590.1:n.969+1795G>C (SGSH)
XR_001752591.1:n.969+1795G>C (SGSH)
XR_001752592.1:n.969+1795G>C (SGSH)
XR_002958057.1:n.1024+1593G>C (SGSH)
NM_000199.5:c.*176G>C (SGSH) MANE Select	NP_000190.1:n.*176G>C
NM_001352921.2:c.*772G>C (SGSH)	NP_001339850.1:n.*772G>C
NM_001352922.2:c.*735G>C (SGSH)	NP_001339851.1:n.*735G>C
NR_148201.2:n.1599G>C (SGSH)
NM_001352921.3:c.*772G>C (SGSH)	NP_001339850.1:n.*772G>C