Canonical Allele Identifier: CA401358591

Gene: CARD14 SGSH

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210594C>G , CM000679.2:g.80210594C>G	GRCh38
NC_000017.10:g.78184393C>G , CM000679.1:g.78184393C>G	GRCh37
NC_000017.9:g.75798988C>G	NCBI36
NG_008229.1:g.14807G>C
NG_032778.1:g.45603C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1336C>G (CARD14)
ENST00000326317.11:c.1367G>C (SGSH) MANE Select	ENSP00000314606.6:p.Arg456Pro
ENST00000326317.10:c.1367G>C (SGSH)	ENSP00000314606.6:p.Arg456Pro
ENST00000572257.5:c.551+1477G>C (SGSH)
ENST00000573150.5:c.*577G>C (SGSH)	ENSP00000459280.1:n.*577G>C
ENST00000575282.5:n.4250G>C (SGSH)
ENST00000576856.1:c.621G>C (SGSH)	ENSP00000460720.1:n.621G>C
NM_000199.3:c.1367G>C (SGSH)	NP_000190.1:p.Arg456Pro
XM_005257583.3:c.949+1477G>C (SGSH)	XP_005257640.1:n.949+1477G>C
NM_000199.4:c.1367G>C (SGSH)	NP_000190.1:p.Arg456Pro
NM_001352921.1:c.*454G>C (SGSH)	NP_001339850.1:n.*454G>C
NM_001352922.1:c.*417G>C (SGSH)	NP_001339851.1:n.*417G>C
NR_148201.1:n.1348G>C (SGSH)
XM_005257583.4:c.949+1477G>C (SGSH)	XP_005257640.1:n.949+1477G>C
XM_017024952.1:c.*1271G>C (SGSH)	XP_016880441.1:n.*1271G>C
XR_001752585.1:n.1387G>C (SGSH)
XR_001752586.1:n.969+1477G>C (SGSH)
XR_001752587.1:n.969+1477G>C (SGSH)
XR_001752588.1:n.969+1477G>C (SGSH)
XR_001752589.1:n.969+1477G>C (SGSH)
XR_001752590.1:n.969+1477G>C (SGSH)
XR_001752591.1:n.969+1477G>C (SGSH)
XR_001752592.1:n.969+1477G>C (SGSH)
XR_002958057.1:n.1024+1275G>C (SGSH)
NM_000199.5:c.1367G>C (SGSH) MANE Select	NP_000190.1:p.Arg456Pro
NM_001352921.2:c.*454G>C (SGSH)	NP_001339850.1:n.*454G>C
NM_001352922.2:c.*417G>C (SGSH)	NP_001339851.1:n.*417G>C
NR_148201.2:n.1281G>C (SGSH)
NM_001352921.3:c.*454G>C (SGSH)	NP_001339850.1:n.*454G>C