Canonical Allele Identifier: CA8817698

Gene: CARD14 SGSH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210959G>A , CM000679.2:g.80210959G>A	GRCh38
NC_000017.10:g.78184758G>A , CM000679.1:g.78184758G>A	GRCh37
NC_000017.9:g.75799353G>A	NCBI36
NG_008229.1:g.14442C>T
NG_032778.1:g.45968G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1701G>A (CARD14)
ENST00000326317.11:c.1002C>T (SGSH) MANE Select	ENSP00000314606.6:p.Ala334=
ENST00000326317.10:c.1002C>T (SGSH)	ENSP00000314606.6:p.Ala334=
ENST00000572257.5:c.551+1112C>T (SGSH)
ENST00000573150.5:c.*212C>T (SGSH)	ENSP00000459280.1:n.*212C>T
ENST00000575282.5:n.3885C>T (SGSH)
ENST00000576856.1:c.256C>T (SGSH)	ENSP00000460720.1:n.256C>T
NM_000199.3:c.1002C>T (SGSH)	NP_000190.1:p.Ala334=
XM_005257582.2:c.*89C>T (SGSH)	XP_005257639.1:n.*89C>T
XM_005257583.3:c.949+1112C>T (SGSH)	XP_005257640.1:n.949+1112C>T
XM_011525127.1:c.*52C>T (SGSH)	XP_011523429.1:n.*52C>T
NM_000199.4:c.1002C>T (SGSH)	NP_000190.1:p.Ala334=
NM_001352921.1:c.*89C>T (SGSH)	NP_001339850.1:n.*89C>T
NM_001352922.1:c.*52C>T (SGSH)	NP_001339851.1:n.*52C>T
NR_148201.1:n.983C>T (SGSH)
XM_005257583.4:c.949+1112C>T (SGSH)	XP_005257640.1:n.949+1112C>T
XM_017024952.1:c.*906C>T (SGSH)	XP_016880441.1:n.*906C>T
XR_001752585.1:n.1022C>T (SGSH)
XR_001752586.1:n.969+1112C>T (SGSH)
XR_001752587.1:n.969+1112C>T (SGSH)
XR_001752588.1:n.969+1112C>T (SGSH)
XR_001752589.1:n.969+1112C>T (SGSH)
XR_001752590.1:n.969+1112C>T (SGSH)
XR_001752591.1:n.969+1112C>T (SGSH)
XR_001752592.1:n.969+1112C>T (SGSH)
XR_002958057.1:n.1024+910C>T (SGSH)
NM_000199.5:c.1002C>T (SGSH) MANE Select	NP_000190.1:p.Ala334=
NM_001352921.2:c.*89C>T (SGSH)	NP_001339850.1:n.*89C>T
NM_001352922.2:c.*52C>T (SGSH)	NP_001339851.1:n.*52C>T
NR_148201.2:n.916C>T (SGSH)
NM_001352921.3:c.*89C>T (SGSH)	NP_001339850.1:n.*89C>T