Canonical Allele Identifier: CA401364738

Gene: SGSH

Linked Data

• MyVariant Identifiers: chr17:g.78190980C>G (hg19) ; chr17:g.80217181C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217181C>G , CM000679.2:g.80217181C>G	GRCh38
NC_000017.10:g.78190980C>G , CM000679.1:g.78190980C>G	GRCh37
NC_000017.9:g.75805575C>G	NCBI36
NG_008229.1:g.8220G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.100G>C MANE Select	ENSP00000314606.6:p.Gly34Arg
ENST00000326317.10:c.100G>C	ENSP00000314606.6:p.Gly34Arg
ENST00000570427.1:c.100G>C	ENSP00000459765.1:p.Gly34Arg
ENST00000570923.1:c.135G>C	ENSP00000458200.1:p.Glu45Asp
ENST00000571051.5:n.120G>C
ENST00000571075.1:n.120G>C
ENST00000571675.5:n.120G>C
ENST00000572208.5:n.118G>C
ENST00000573150.5:c.100G>C	ENSP00000459280.1:p.Gly34Arg
ENST00000574505.5:c.45G>C
ENST00000575188.5:n.120G>C
ENST00000575282.5:n.109G>C
ENST00000576707.5:c.-162G>C	ENSP00000461128.1:n.-162G>C
ENST00000576941.5:c.100G>C	ENSP00000461160.1:p.Gly34Arg
NM_000199.3:c.100G>C	NP_000190.1:p.Gly34Arg
XM_005257582.2:c.100G>C	XP_005257639.1:p.Gly34Arg
XM_005257583.3:c.100G>C	XP_005257640.1:p.Gly34Arg
XM_011525126.1:c.100G>C	XP_011523428.1:p.Gly34Arg
XM_011525127.1:c.100G>C	XP_011523429.1:p.Gly34Arg
XR_934532.1:n.120G>C
NM_000199.4:c.100G>C	NP_000190.1:p.Gly34Arg
NM_001352921.1:c.100G>C	NP_001339850.1:p.Gly34Arg
NM_001352922.1:c.100G>C	NP_001339851.1:p.Gly34Arg
NR_148201.1:n.187G>C
XM_005257583.4:c.100G>C	XP_005257640.1:p.Gly34Arg
XM_017024952.1:c.100G>C	XP_016880441.1:p.Gly34Arg
XR_001752585.1:n.120G>C
XR_001752586.1:n.120G>C
XR_001752587.1:n.120G>C
XR_001752588.1:n.120G>C
XR_001752589.1:n.120G>C
XR_001752590.1:n.120G>C
XR_001752591.1:n.120G>C
XR_001752592.1:n.120G>C
XR_002958057.1:n.120G>C
XR_934532.2:n.120G>C
NM_000199.5:c.100G>C MANE Select	NP_000190.1:p.Gly34Arg
NM_001352921.2:c.100G>C	NP_001339850.1:p.Gly34Arg
NM_001352922.2:c.100G>C	NP_001339851.1:p.Gly34Arg
NR_148201.2:n.120G>C
NM_001352921.3:c.100G>C	NP_001339850.1:p.Gly34Arg