Canonical Allele Identifier: CA401358638

Gene: CARD14 SGSH

Linked Data

• MyVariant Identifiers: chr17:g.78184417G>C (hg19) ; chr17:g.80210618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210618G>C , CM000679.2:g.80210618G>C	GRCh38
NC_000017.10:g.78184417G>C , CM000679.1:g.78184417G>C	GRCh37
NC_000017.9:g.75799012G>C	NCBI36
NG_008229.1:g.14783C>G
NG_032778.1:g.45627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1360G>C (CARD14)
ENST00000326317.11:c.1343C>G (SGSH) MANE Select	ENSP00000314606.6:p.Thr448Ser
ENST00000326317.10:c.1343C>G (SGSH)	ENSP00000314606.6:p.Thr448Ser
ENST00000572257.5:c.551+1453C>G (SGSH)
ENST00000573150.5:c.*553C>G (SGSH)	ENSP00000459280.1:n.*553C>G
ENST00000575282.5:n.4226C>G (SGSH)
ENST00000576856.1:c.597C>G (SGSH)	ENSP00000460720.1:n.597C>G
NM_000199.3:c.1343C>G (SGSH)	NP_000190.1:p.Thr448Ser
XM_005257583.3:c.949+1453C>G (SGSH)	XP_005257640.1:n.949+1453C>G
NM_000199.4:c.1343C>G (SGSH)	NP_000190.1:p.Thr448Ser
NM_001352921.1:c.*430C>G (SGSH)	NP_001339850.1:n.*430C>G
NM_001352922.1:c.*393C>G (SGSH)	NP_001339851.1:n.*393C>G
NR_148201.1:n.1324C>G (SGSH)
XM_005257583.4:c.949+1453C>G (SGSH)	XP_005257640.1:n.949+1453C>G
XM_017024952.1:c.*1247C>G (SGSH)	XP_016880441.1:n.*1247C>G
XR_001752585.1:n.1363C>G (SGSH)
XR_001752586.1:n.969+1453C>G (SGSH)
XR_001752587.1:n.969+1453C>G (SGSH)
XR_001752588.1:n.969+1453C>G (SGSH)
XR_001752589.1:n.969+1453C>G (SGSH)
XR_001752590.1:n.969+1453C>G (SGSH)
XR_001752591.1:n.969+1453C>G (SGSH)
XR_001752592.1:n.969+1453C>G (SGSH)
XR_002958057.1:n.1024+1251C>G (SGSH)
NM_000199.5:c.1343C>G (SGSH) MANE Select	NP_000190.1:p.Thr448Ser
NM_001352921.2:c.*430C>G (SGSH)	NP_001339850.1:n.*430C>G
NM_001352922.2:c.*393C>G (SGSH)	NP_001339851.1:n.*393C>G
NR_148201.2:n.1257C>G (SGSH)
NM_001352921.3:c.*430C>G (SGSH)	NP_001339850.1:n.*430C>G