Canonical Allele Identifier: CA401358648

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210622C>G , CM000679.2:g.80210622C>G	GRCh38
NC_000017.10:g.78184421C>G , CM000679.1:g.78184421C>G	GRCh37
NC_000017.9:g.75799016C>G	NCBI36
NG_008229.1:g.14779G>C
NG_032778.1:g.45631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+1364C>G (CARD14)
ENST00000326317.11:c.1339G>C (SGSH) MANE Select	ENSP00000314606.6:p.Glu447Gln
ENST00000326317.10:c.1339G>C (SGSH)	ENSP00000314606.6:p.Glu447Gln
ENST00000572257.5:c.551+1449G>C (SGSH)
ENST00000573150.5:c.*549G>C (SGSH)	ENSP00000459280.1:n.*549G>C
ENST00000575282.5:n.4222G>C (SGSH)
ENST00000576856.1:c.593G>C (SGSH)	ENSP00000460720.1:n.593G>C
NM_000199.3:c.1339G>C (SGSH)	NP_000190.1:p.Glu447Gln
XM_005257583.3:c.949+1449G>C (SGSH)	XP_005257640.1:n.949+1449G>C
NM_000199.4:c.1339G>C (SGSH)	NP_000190.1:p.Glu447Gln
NM_001352921.1:c.*426G>C (SGSH)	NP_001339850.1:n.*426G>C
NM_001352922.1:c.*389G>C (SGSH)	NP_001339851.1:n.*389G>C
NR_148201.1:n.1320G>C (SGSH)
XM_005257583.4:c.949+1449G>C (SGSH)	XP_005257640.1:n.949+1449G>C
XM_017024952.1:c.*1243G>C (SGSH)	XP_016880441.1:n.*1243G>C
XR_001752585.1:n.1359G>C (SGSH)
XR_001752586.1:n.969+1449G>C (SGSH)
XR_001752587.1:n.969+1449G>C (SGSH)
XR_001752588.1:n.969+1449G>C (SGSH)
XR_001752589.1:n.969+1449G>C (SGSH)
XR_001752590.1:n.969+1449G>C (SGSH)
XR_001752591.1:n.969+1449G>C (SGSH)
XR_001752592.1:n.969+1449G>C (SGSH)
XR_002958057.1:n.1024+1247G>C (SGSH)
NM_000199.5:c.1339G>C (SGSH) MANE Select	NP_000190.1:p.Glu447Gln
NM_001352921.2:c.*426G>C (SGSH)	NP_001339850.1:n.*426G>C
NM_001352922.2:c.*389G>C (SGSH)	NP_001339851.1:n.*389G>C
NR_148201.2:n.1253G>C (SGSH)
NM_001352921.3:c.*426G>C (SGSH)	NP_001339850.1:n.*426G>C