Canonical Allele Identifier: CA2277865347

Gene: SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217211A= , CM000679.2:g.80217211A=	GRCh38
NC_000017.10:g.78191010A= , CM000679.1:g.78191010A=	GRCh37
NC_000017.9:g.75805605A=	NCBI36
NG_008229.1:g.8190T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.89-19T= MANE Select	ENSP00000314606.6:n.89-19T=
ENST00000326317.10:c.89-19T=	ENSP00000314606.6:n.89-19T=
ENST00000570427.1:c.89-19T=	ENSP00000459765.1:n.89-19T=
ENST00000570923.1:c.105T=	ENSP00000458200.1:p.Ser35=
ENST00000571051.5:n.109-19T=
ENST00000571075.1:n.109-19T=
ENST00000571675.5:n.109-19T=
ENST00000572208.5:n.107-19T=
ENST00000573150.5:c.89-19T=	ENSP00000459280.1:n.89-19T=
ENST00000574505.5:c.34-19T=
ENST00000575188.5:n.109-19T=
ENST00000575282.5:n.98-19T=
ENST00000576707.5:c.-173-19T=	ENSP00000461128.1:n.-173-19T=
ENST00000576941.5:c.89-19T=	ENSP00000461160.1:n.89-19T=
NM_000199.3:c.89-19T=	NP_000190.1:n.89-19T=
XM_005257582.2:c.89-19T=	XP_005257639.1:n.89-19T=
XM_005257583.3:c.89-19T=	XP_005257640.1:n.89-19T=
XM_011525126.1:c.89-19T=	XP_011523428.1:n.89-19T=
XM_011525127.1:c.89-19T=	XP_011523429.1:n.89-19T=
XR_934532.1:n.109-19T=
NM_000199.4:c.89-19T=	NP_000190.1:n.89-19T=
NM_001352921.1:c.89-19T=	NP_001339850.1:n.89-19T=
NM_001352922.1:c.89-19T=	NP_001339851.1:n.89-19T=
NR_148201.1:n.176-19T=
XM_005257583.4:c.89-19T=	XP_005257640.1:n.89-19T=
XM_017024952.1:c.89-19T=	XP_016880441.1:n.89-19T=
XR_001752585.1:n.109-19T=
XR_001752586.1:n.109-19T=
XR_001752587.1:n.109-19T=
XR_001752588.1:n.109-19T=
XR_001752589.1:n.109-19T=
XR_001752590.1:n.109-19T=
XR_001752591.1:n.109-19T=
XR_001752592.1:n.109-19T=
XR_002958057.1:n.109-19T=
XR_934532.2:n.109-19T=
NM_000199.5:c.89-19T= MANE Select	NP_000190.1:n.89-19T=
NM_001352921.2:c.89-19T=	NP_001339850.1:n.89-19T=
NM_001352922.2:c.89-19T=	NP_001339851.1:n.89-19T=
NR_148201.2:n.109-19T=
NM_001352921.3:c.89-19T=	NP_001339850.1:n.89-19T=