Canonical Allele Identifier: CA401364633
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 551665
ClinVar RCV Id: RCV000666789
dbSNP Id: rs1555623007

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80217162T>G , CM000679.2:g.80217162T>G GRCh38
NC_000017.10:g.78190961T>G , CM000679.1:g.78190961T>G GRCh37
NC_000017.9:g.75805556T>G NCBI36
NG_008229.1:g.8239A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000326317.11:c.119A>C MANE Select ENSP00000314606.6:p.Tyr40Ser
ENST00000326317.10:c.119A>C ENSP00000314606.6:p.Tyr40Ser
ENST00000570427.1:c.119A>C ENSP00000459765.1:p.Tyr40Ser
ENST00000570923.1:c.154A>C ENSP00000458200.1:p.Thr52Pro
ENST00000571051.5:n.139A>C
ENST00000571075.1:n.139A>C
ENST00000571675.5:n.139A>C
ENST00000572208.5:n.137A>C
ENST00000573150.5:c.119A>C ENSP00000459280.1:p.Tyr40Ser
ENST00000574505.5:c.64A>C
ENST00000575188.5:n.139A>C
ENST00000575282.5:n.128A>C
ENST00000576707.5:c.-143A>C ENSP00000461128.1:n.-143A>C
ENST00000576941.5:c.119A>C ENSP00000461160.1:p.Tyr40Ser
NM_000199.3:c.119A>C NP_000190.1:p.Tyr40Ser
XM_005257582.2:c.119A>C XP_005257639.1:p.Tyr40Ser
XM_005257583.3:c.119A>C XP_005257640.1:p.Tyr40Ser
XM_011525126.1:c.119A>C XP_011523428.1:p.Tyr40Ser
XM_011525127.1:c.119A>C XP_011523429.1:p.Tyr40Ser
XR_934532.1:n.139A>C
NM_000199.4:c.119A>C NP_000190.1:p.Tyr40Ser
NM_001352921.1:c.119A>C NP_001339850.1:p.Tyr40Ser
NM_001352922.1:c.119A>C NP_001339851.1:p.Tyr40Ser
NR_148201.1:n.206A>C
XM_005257583.4:c.119A>C XP_005257640.1:p.Tyr40Ser
XM_017024952.1:c.119A>C XP_016880441.1:p.Tyr40Ser
XR_001752585.1:n.139A>C
XR_001752586.1:n.139A>C
XR_001752587.1:n.139A>C
XR_001752588.1:n.139A>C
XR_001752589.1:n.139A>C
XR_001752590.1:n.139A>C
XR_001752591.1:n.139A>C
XR_001752592.1:n.139A>C
XR_002958057.1:n.139A>C
XR_934532.2:n.139A>C
NM_000199.5:c.119A>C MANE Select NP_000190.1:p.Tyr40Ser
NM_001352921.2:c.119A>C NP_001339850.1:p.Tyr40Ser
NM_001352922.2:c.119A>C NP_001339851.1:p.Tyr40Ser
NR_148201.2:n.139A>C
NM_001352921.3:c.119A>C NP_001339850.1:p.Tyr40Ser