Canonical Allele Identifier: CA401364601

Gene: SGSH

Linked Data

• MyVariant Identifiers: chr17:g.78190955T>G (hg19) ; chr17:g.80217156T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217156T>G , CM000679.2:g.80217156T>G	GRCh38
NC_000017.10:g.78190955T>G , CM000679.1:g.78190955T>G	GRCh37
NC_000017.9:g.75805550T>G	NCBI36
NG_008229.1:g.8245A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.125A>C MANE Select	ENSP00000314606.6:p.Asn42Thr
ENST00000326317.10:c.125A>C	ENSP00000314606.6:p.Asn42Thr
ENST00000570427.1:c.125A>C	ENSP00000459765.1:p.Asn42Thr
ENST00000570923.1:c.160A>C	ENSP00000458200.1:p.Thr54Pro
ENST00000571051.5:n.145A>C
ENST00000571075.1:n.145A>C
ENST00000571675.5:n.145A>C
ENST00000572208.5:n.143A>C
ENST00000573150.5:c.125A>C	ENSP00000459280.1:p.Asn42Thr
ENST00000574505.5:c.70A>C
ENST00000575188.5:n.145A>C
ENST00000575282.5:n.134A>C
ENST00000576707.5:c.-137A>C	ENSP00000461128.1:n.-137A>C
ENST00000576941.5:c.125A>C	ENSP00000461160.1:p.Asn42Thr
NM_000199.3:c.125A>C	NP_000190.1:p.Asn42Thr
XM_005257582.2:c.125A>C	XP_005257639.1:p.Asn42Thr
XM_005257583.3:c.125A>C	XP_005257640.1:p.Asn42Thr
XM_011525126.1:c.125A>C	XP_011523428.1:p.Asn42Thr
XM_011525127.1:c.125A>C	XP_011523429.1:p.Asn42Thr
XR_934532.1:n.145A>C
NM_000199.4:c.125A>C	NP_000190.1:p.Asn42Thr
NM_001352921.1:c.125A>C	NP_001339850.1:p.Asn42Thr
NM_001352922.1:c.125A>C	NP_001339851.1:p.Asn42Thr
NR_148201.1:n.212A>C
XM_005257583.4:c.125A>C	XP_005257640.1:p.Asn42Thr
XM_017024952.1:c.125A>C	XP_016880441.1:p.Asn42Thr
XR_001752585.1:n.145A>C
XR_001752586.1:n.145A>C
XR_001752587.1:n.145A>C
XR_001752588.1:n.145A>C
XR_001752589.1:n.145A>C
XR_001752590.1:n.145A>C
XR_001752591.1:n.145A>C
XR_001752592.1:n.145A>C
XR_002958057.1:n.145A>C
XR_934532.2:n.145A>C
NM_000199.5:c.125A>C MANE Select	NP_000190.1:p.Asn42Thr
NM_001352921.2:c.125A>C	NP_001339850.1:p.Asn42Thr
NM_001352922.2:c.125A>C	NP_001339851.1:p.Asn42Thr
NR_148201.2:n.145A>C
NM_001352921.3:c.125A>C	NP_001339850.1:p.Asn42Thr