Canonical Allele Identifier: CA294890188

Gene: CARD14 SGSH

Linked Data

• dbSNP Id: rs770317133
• gnomAD v4: 17-80210286-T-C
• MyVariant Identifiers: chr17:g.78184085T>C (hg19) ; chr17:g.80210286T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210286T>C , CM000679.2:g.80210286T>C	GRCh38
NC_000017.10:g.78184085T>C , CM000679.1:g.78184085T>C	GRCh37
NC_000017.9:g.75798680T>C	NCBI36
NG_008229.1:g.15115A>G
NG_032778.1:g.45295T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1028T>C (CARD14)
ENST00000326317.11:c.*166A>G (SGSH) MANE Select	ENSP00000314606.6:n.*166A>G
ENST00000326317.10:c.*166A>G (SGSH)	ENSP00000314606.6:n.*166A>G
ENST00000572257.5:c.551+1785A>G (SGSH)
ENST00000573150.5:c.*885A>G (SGSH)	ENSP00000459280.1:n.*885A>G
ENST00000575282.5:n.4558A>G (SGSH)
NM_000199.3:c.*166A>G (SGSH)	NP_000190.1:n.*166A>G
XM_005257583.3:c.949+1785A>G (SGSH)	XP_005257640.1:n.949+1785A>G
NM_000199.4:c.*166A>G (SGSH)	NP_000190.1:n.*166A>G
NM_001352921.1:c.*762A>G (SGSH)	NP_001339850.1:n.*762A>G
NM_001352922.1:c.*725A>G (SGSH)	NP_001339851.1:n.*725A>G
NR_148201.1:n.1656A>G (SGSH)
XM_005257583.4:c.949+1785A>G (SGSH)	XP_005257640.1:n.949+1785A>G
XM_017024952.1:c.*1579A>G (SGSH)	XP_016880441.1:n.*1579A>G
XR_001752585.1:n.1695A>G (SGSH)
XR_001752586.1:n.969+1785A>G (SGSH)
XR_001752587.1:n.969+1785A>G (SGSH)
XR_001752588.1:n.969+1785A>G (SGSH)
XR_001752589.1:n.969+1785A>G (SGSH)
XR_001752590.1:n.969+1785A>G (SGSH)
XR_001752591.1:n.969+1785A>G (SGSH)
XR_001752592.1:n.969+1785A>G (SGSH)
XR_002958057.1:n.1024+1583A>G (SGSH)
NM_000199.5:c.*166A>G (SGSH) MANE Select	NP_000190.1:n.*166A>G
NM_001352921.2:c.*762A>G (SGSH)	NP_001339850.1:n.*762A>G
NM_001352922.2:c.*725A>G (SGSH)	NP_001339851.1:n.*725A>G
NR_148201.2:n.1589A>G (SGSH)
NM_001352921.3:c.*762A>G (SGSH)	NP_001339850.1:n.*762A>G