Canonical Allele Identifier: CA2277865240

Gene: SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217161G= , CM000679.2:g.80217161G=	GRCh38
NC_000017.10:g.78190960G= , CM000679.1:g.78190960G=	GRCh37
NC_000017.9:g.75805555G=	NCBI36
NG_008229.1:g.8240C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.120C= MANE Select	ENSP00000314606.6:p.Tyr40=
ENST00000326317.10:c.120C=	ENSP00000314606.6:p.Tyr40=
ENST00000570427.1:c.120C=	ENSP00000459765.1:p.Tyr40=
ENST00000570923.1:c.155C=	ENSP00000458200.1:p.Thr52=
ENST00000571051.5:n.140C=
ENST00000571075.1:n.140C=
ENST00000571675.5:n.140C=
ENST00000572208.5:n.138C=
ENST00000573150.5:c.120C=	ENSP00000459280.1:p.Tyr40=
ENST00000574505.5:c.65C=
ENST00000575188.5:n.140C=
ENST00000575282.5:n.129C=
ENST00000576707.5:c.-142C=	ENSP00000461128.1:n.-142C=
ENST00000576941.5:c.120C=	ENSP00000461160.1:p.Tyr40=
NM_000199.3:c.120C=	NP_000190.1:p.Tyr40=
XM_005257582.2:c.120C=	XP_005257639.1:p.Tyr40=
XM_005257583.3:c.120C=	XP_005257640.1:p.Tyr40=
XM_011525126.1:c.120C=	XP_011523428.1:p.Tyr40=
XM_011525127.1:c.120C=	XP_011523429.1:p.Tyr40=
XR_934532.1:n.140C=
NM_000199.4:c.120C=	NP_000190.1:p.Tyr40=
NM_001352921.1:c.120C=	NP_001339850.1:p.Tyr40=
NM_001352922.1:c.120C=	NP_001339851.1:p.Tyr40=
NR_148201.1:n.207C=
XM_005257583.4:c.120C=	XP_005257640.1:p.Tyr40=
XM_017024952.1:c.120C=	XP_016880441.1:p.Tyr40=
XR_001752585.1:n.140C=
XR_001752586.1:n.140C=
XR_001752587.1:n.140C=
XR_001752588.1:n.140C=
XR_001752589.1:n.140C=
XR_001752590.1:n.140C=
XR_001752591.1:n.140C=
XR_001752592.1:n.140C=
XR_002958057.1:n.140C=
XR_934532.2:n.140C=
NM_000199.5:c.120C= MANE Select	NP_000190.1:p.Tyr40=
NM_001352921.2:c.120C=	NP_001339850.1:p.Tyr40=
NM_001352922.2:c.120C=	NP_001339851.1:p.Tyr40=
NR_148201.2:n.140C=
NM_001352921.3:c.120C=	NP_001339850.1:p.Tyr40=