Canonical Allele Identifier: CA401364586
Gene: SGSH HGNC NCBI

Linked Data

dbSNP Id: rs1291601158

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80217154T>C , CM000679.2:g.80217154T>C GRCh38
NC_000017.10:g.78190953T>C , CM000679.1:g.78190953T>C GRCh37
NC_000017.9:g.75805548T>C NCBI36
NG_008229.1:g.8247A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000326317.11:c.127A>G MANE Select ENSP00000314606.6:p.Ser43Gly
ENST00000326317.10:c.127A>G ENSP00000314606.6:p.Ser43Gly
ENST00000570427.1:c.127A>G ENSP00000459765.1:p.Ser43Gly
ENST00000570923.1:c.162A>G ENSP00000458200.1:p.Thr54=
ENST00000571051.5:n.147A>G
ENST00000571075.1:n.147A>G
ENST00000571675.5:n.147A>G
ENST00000572208.5:n.145A>G
ENST00000573150.5:c.127A>G ENSP00000459280.1:p.Ser43Gly
ENST00000574505.5:c.72A>G
ENST00000575188.5:n.147A>G
ENST00000575282.5:n.136A>G
ENST00000576707.5:c.-135A>G ENSP00000461128.1:n.-135A>G
ENST00000576941.5:c.127A>G ENSP00000461160.1:p.Ser43Gly
NM_000199.3:c.127A>G NP_000190.1:p.Ser43Gly
XM_005257582.2:c.127A>G XP_005257639.1:p.Ser43Gly
XM_005257583.3:c.127A>G XP_005257640.1:p.Ser43Gly
XM_011525126.1:c.127A>G XP_011523428.1:p.Ser43Gly
XM_011525127.1:c.127A>G XP_011523429.1:p.Ser43Gly
XR_934532.1:n.147A>G
NM_000199.4:c.127A>G NP_000190.1:p.Ser43Gly
NM_001352921.1:c.127A>G NP_001339850.1:p.Ser43Gly
NM_001352922.1:c.127A>G NP_001339851.1:p.Ser43Gly
NR_148201.1:n.214A>G
XM_005257583.4:c.127A>G XP_005257640.1:p.Ser43Gly
XM_017024952.1:c.127A>G XP_016880441.1:p.Ser43Gly
XR_001752585.1:n.147A>G
XR_001752586.1:n.147A>G
XR_001752587.1:n.147A>G
XR_001752588.1:n.147A>G
XR_001752589.1:n.147A>G
XR_001752590.1:n.147A>G
XR_001752591.1:n.147A>G
XR_001752592.1:n.147A>G
XR_002958057.1:n.147A>G
XR_934532.2:n.147A>G
NM_000199.5:c.127A>G MANE Select NP_000190.1:p.Ser43Gly
NM_001352921.2:c.127A>G NP_001339850.1:p.Ser43Gly
NM_001352922.2:c.127A>G NP_001339851.1:p.Ser43Gly
NR_148201.2:n.147A>G
NM_001352921.3:c.127A>G NP_001339850.1:p.Ser43Gly