Canonical Allele Identifier: CA401364372

Gene: SGSH

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217112T>G , CM000679.2:g.80217112T>G	GRCh38
NC_000017.10:g.78190911T>G , CM000679.1:g.78190911T>G	GRCh37
NC_000017.9:g.75805506T>G	NCBI36
NG_008229.1:g.8289A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.169A>C MANE Select	ENSP00000314606.6:p.Ser57Arg
ENST00000326317.10:c.169A>C	ENSP00000314606.6:p.Ser57Arg
ENST00000570427.1:c.169A>C	ENSP00000459765.1:p.Ser57Arg
ENST00000570923.1:c.204A>C	ENSP00000458200.1:p.Ala68=
ENST00000571051.5:n.189A>C
ENST00000571075.1:n.189A>C
ENST00000571675.5:n.189A>C
ENST00000572208.5:n.187A>C
ENST00000573150.5:c.169A>C	ENSP00000459280.1:p.Ser57Arg
ENST00000574505.5:c.114A>C
ENST00000575188.5:n.189A>C
ENST00000575282.5:n.178A>C
ENST00000576707.5:c.-93A>C	ENSP00000461128.1:n.-93A>C
ENST00000576941.5:c.169A>C	ENSP00000461160.1:p.Ser57Arg
NM_000199.3:c.169A>C	NP_000190.1:p.Ser57Arg
XM_005257582.2:c.169A>C	XP_005257639.1:p.Ser57Arg
XM_005257583.3:c.169A>C	XP_005257640.1:p.Ser57Arg
XM_011525126.1:c.169A>C	XP_011523428.1:p.Ser57Arg
XM_011525127.1:c.169A>C	XP_011523429.1:p.Ser57Arg
XR_934532.1:n.189A>C
NM_000199.4:c.169A>C	NP_000190.1:p.Ser57Arg
NM_001352921.1:c.169A>C	NP_001339850.1:p.Ser57Arg
NM_001352922.1:c.169A>C	NP_001339851.1:p.Ser57Arg
NR_148201.1:n.256A>C
XM_005257583.4:c.169A>C	XP_005257640.1:p.Ser57Arg
XM_017024952.1:c.169A>C	XP_016880441.1:p.Ser57Arg
XR_001752585.1:n.189A>C
XR_001752586.1:n.189A>C
XR_001752587.1:n.189A>C
XR_001752588.1:n.189A>C
XR_001752589.1:n.189A>C
XR_001752590.1:n.189A>C
XR_001752591.1:n.189A>C
XR_001752592.1:n.189A>C
XR_002958057.1:n.189A>C
XR_934532.2:n.189A>C
NM_000199.5:c.169A>C MANE Select	NP_000190.1:p.Ser57Arg
NM_001352921.2:c.169A>C	NP_001339850.1:p.Ser57Arg
NM_001352922.2:c.169A>C	NP_001339851.1:p.Ser57Arg
NR_148201.2:n.189A>C
NM_001352921.3:c.169A>C	NP_001339850.1:p.Ser57Arg