Canonical Allele Identifier: CA2640319782

Gene: CARD14 SGSH

Linked Data

• gnomAD v4: 17-80210397-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210397G>T , CM000679.2:g.80210397G>T	GRCh38
NC_000017.10:g.78184196G>T , CM000679.1:g.78184196G>T	GRCh37
NC_000017.9:g.75798791G>T	NCBI36
NG_008229.1:g.15004C>A
NG_032778.1:g.45406G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1139G>T (CARD14)
ENST00000326317.11:c.*55C>A (SGSH) MANE Select	ENSP00000314606.6:n.*55C>A
ENST00000326317.10:c.*55C>A (SGSH)	ENSP00000314606.6:n.*55C>A
ENST00000572257.5:c.551+1674C>A (SGSH)
ENST00000573150.5:c.*774C>A (SGSH)	ENSP00000459280.1:n.*774C>A
ENST00000575282.5:n.4447C>A (SGSH)
ENST00000576856.1:c.818C>A (SGSH)	ENSP00000460720.1:n.818C>A
NM_000199.3:c.*55C>A (SGSH)	NP_000190.1:n.*55C>A
XM_005257583.3:c.949+1674C>A (SGSH)	XP_005257640.1:n.949+1674C>A
NM_000199.4:c.*55C>A (SGSH)	NP_000190.1:n.*55C>A
NM_001352921.1:c.*651C>A (SGSH)	NP_001339850.1:n.*651C>A
NM_001352922.1:c.*614C>A (SGSH)	NP_001339851.1:n.*614C>A
NR_148201.1:n.1545C>A (SGSH)
XM_005257583.4:c.949+1674C>A (SGSH)	XP_005257640.1:n.949+1674C>A
XM_017024952.1:c.*1468C>A (SGSH)	XP_016880441.1:n.*1468C>A
XR_001752585.1:n.1584C>A (SGSH)
XR_001752586.1:n.969+1674C>A (SGSH)
XR_001752587.1:n.969+1674C>A (SGSH)
XR_001752588.1:n.969+1674C>A (SGSH)
XR_001752589.1:n.969+1674C>A (SGSH)
XR_001752590.1:n.969+1674C>A (SGSH)
XR_001752591.1:n.969+1674C>A (SGSH)
XR_001752592.1:n.969+1674C>A (SGSH)
XR_002958057.1:n.1024+1472C>A (SGSH)
NM_000199.5:c.*55C>A (SGSH) MANE Select	NP_000190.1:n.*55C>A
NM_001352921.2:c.*651C>A (SGSH)	NP_001339850.1:n.*651C>A
NM_001352922.2:c.*614C>A (SGSH)	NP_001339851.1:n.*614C>A
NR_148201.2:n.1478C>A (SGSH)
NM_001352921.3:c.*651C>A (SGSH)	NP_001339850.1:n.*651C>A