Canonical Allele Identifier: CA2640318908

Gene: CARD14 SGSH

Linked Data

• gnomAD v4: 17-80210103-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210103A>C , CM000679.2:g.80210103A>C	GRCh38
NC_000017.10:g.78183902A>C , CM000679.1:g.78183902A>C	GRCh37
NC_000017.9:g.75798497A>C	NCBI36
NG_008229.1:g.15298T>G
NG_032778.1:g.45112A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+845A>C (CARD14)
ENST00000326317.11:c.*349T>G (SGSH) MANE Select	ENSP00000314606.6:n.*349T>G
ENST00000326317.10:c.*349T>G (SGSH)	ENSP00000314606.6:n.*349T>G
ENST00000572257.5:c.551+1968T>G (SGSH)
ENST00000573150.5:c.*1068T>G (SGSH)	ENSP00000459280.1:n.*1068T>G
ENST00000575282.5:n.4741T>G (SGSH)
NM_000199.3:c.*349T>G (SGSH)	NP_000190.1:n.*349T>G
XM_005257583.3:c.949+1968T>G (SGSH)	XP_005257640.1:n.949+1968T>G
NM_000199.4:c.*349T>G (SGSH)	NP_000190.1:n.*349T>G
NM_001352921.1:c.*945T>G (SGSH)	NP_001339850.1:n.*945T>G
NM_001352922.1:c.*908T>G (SGSH)	NP_001339851.1:n.*908T>G
NR_148201.1:n.1839T>G (SGSH)
XM_005257583.4:c.949+1968T>G (SGSH)	XP_005257640.1:n.949+1968T>G
XM_017024952.1:c.*1762T>G (SGSH)	XP_016880441.1:n.*1762T>G
XR_001752585.1:n.1878T>G (SGSH)
XR_001752586.1:n.969+1968T>G (SGSH)
XR_001752587.1:n.969+1968T>G (SGSH)
XR_001752588.1:n.969+1968T>G (SGSH)
XR_001752589.1:n.969+1968T>G (SGSH)
XR_001752590.1:n.969+1968T>G (SGSH)
XR_001752591.1:n.969+1968T>G (SGSH)
XR_001752592.1:n.969+1968T>G (SGSH)
XR_002958057.1:n.1024+1766T>G (SGSH)
NM_000199.5:c.*349T>G (SGSH) MANE Select	NP_000190.1:n.*349T>G
NM_001352921.2:c.*945T>G (SGSH)	NP_001339850.1:n.*945T>G
NM_001352922.2:c.*908T>G (SGSH)	NP_001339851.1:n.*908T>G
NR_148201.2:n.1772T>G (SGSH)
NM_001352921.3:c.*945T>G (SGSH)	NP_001339850.1:n.*945T>G