Canonical Allele Identifier: CA2576415365

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210279G>T , CM000679.2:g.80210279G>T	GRCh38
NC_000017.10:g.78184078G>T , CM000679.1:g.78184078G>T	GRCh37
NC_000017.9:g.75798673G>T	NCBI36
NG_008229.1:g.15122C>A
NG_032778.1:g.45288G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1021G>T (CARD14)
ENST00000326317.11:c.*173C>A (SGSH) MANE Select	ENSP00000314606.6:n.*173C>A
ENST00000326317.10:c.*173C>A (SGSH)	ENSP00000314606.6:n.*173C>A
ENST00000572257.5:c.551+1792C>A (SGSH)
ENST00000573150.5:c.*892C>A (SGSH)	ENSP00000459280.1:n.*892C>A
ENST00000575282.5:n.4565C>A (SGSH)
NM_000199.3:c.*173C>A (SGSH)	NP_000190.1:n.*173C>A
XM_005257583.3:c.949+1792C>A (SGSH)	XP_005257640.1:n.949+1792C>A
NM_000199.4:c.*173C>A (SGSH)	NP_000190.1:n.*173C>A
NM_001352921.1:c.*769C>A (SGSH)	NP_001339850.1:n.*769C>A
NM_001352922.1:c.*732C>A (SGSH)	NP_001339851.1:n.*732C>A
NR_148201.1:n.1663C>A (SGSH)
XM_005257583.4:c.949+1792C>A (SGSH)	XP_005257640.1:n.949+1792C>A
XM_017024952.1:c.*1586C>A (SGSH)	XP_016880441.1:n.*1586C>A
XR_001752585.1:n.1702C>A (SGSH)
XR_001752586.1:n.969+1792C>A (SGSH)
XR_001752587.1:n.969+1792C>A (SGSH)
XR_001752588.1:n.969+1792C>A (SGSH)
XR_001752589.1:n.969+1792C>A (SGSH)
XR_001752590.1:n.969+1792C>A (SGSH)
XR_001752591.1:n.969+1792C>A (SGSH)
XR_001752592.1:n.969+1792C>A (SGSH)
XR_002958057.1:n.1024+1590C>A (SGSH)
NM_000199.5:c.*173C>A (SGSH) MANE Select	NP_000190.1:n.*173C>A
NM_001352921.2:c.*769C>A (SGSH)	NP_001339850.1:n.*769C>A
NM_001352922.2:c.*732C>A (SGSH)	NP_001339851.1:n.*732C>A
NR_148201.2:n.1596C>A (SGSH)
NM_001352921.3:c.*769C>A (SGSH)	NP_001339850.1:n.*769C>A