Canonical Allele Identifier: CA401358957

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210773A>C , CM000679.2:g.80210773A>C	GRCh38
NC_000017.10:g.78184572A>C , CM000679.1:g.78184572A>C	GRCh37
NC_000017.9:g.75799167A>C	NCBI36
NG_008229.1:g.14628T>G
NG_032778.1:g.45782A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000199.5:c.1188T>G (SGSH) MANE Select	NP_000190.1:p.Phe396Leu
ENST00000326317.11:c.1188T>G (SGSH) MANE Select	ENSP00000314606.6:p.Phe396Leu
NM_000199.3:c.1188T>G (SGSH)	NP_000190.1:p.Phe396Leu
NM_000199.4:c.1188T>G (SGSH)	NP_000190.1:p.Phe396Leu
NM_001352921.1:c.*275T>G (SGSH)	NP_001339850.1:n.*275T>G
NM_001352921.2:c.*275T>G (SGSH)	NP_001339850.1:n.*275T>G
NM_001352921.3:c.*275T>G (SGSH)	NP_001339850.1:n.*275T>G
NM_001352922.1:c.*238T>G (SGSH)	NP_001339851.1:n.*238T>G
NM_001352922.2:c.*238T>G (SGSH)	NP_001339851.1:n.*238T>G
NR_148201.1:n.1169T>G (SGSH)
NR_148201.2:n.1102T>G (SGSH)
ENST00000326317.10:c.1188T>G (SGSH)	ENSP00000314606.6:p.Phe396Leu
ENST00000572257.5:c.551+1298T>G (SGSH)
ENST00000573150.5:c.*398T>G (SGSH)	ENSP00000459280.1:n.*398T>G
ENST00000575282.5:n.4071T>G (SGSH)
ENST00000576856.1:c.442T>G (SGSH)	ENSP00000460720.1:n.442T>G
ENST00000703570.1:n.2844+1515A>C (CARD14)
XM_005257583.3:c.949+1298T>G (SGSH)	XP_005257640.1:n.949+1298T>G
XM_005257583.4:c.949+1298T>G (SGSH)	XP_005257640.1:n.949+1298T>G
XM_017024952.1:c.*1092T>G (SGSH)	XP_016880441.1:n.*1092T>G
XR_001752585.1:n.1208T>G (SGSH)
XR_001752586.1:n.969+1298T>G (SGSH)
XR_001752587.1:n.969+1298T>G (SGSH)
XR_001752588.1:n.969+1298T>G (SGSH)
XR_001752589.1:n.969+1298T>G (SGSH)
XR_001752590.1:n.969+1298T>G (SGSH)
XR_001752591.1:n.969+1298T>G (SGSH)
XR_001752592.1:n.969+1298T>G (SGSH)
XR_002958057.1:n.1024+1096T>G (SGSH)