Canonical Allele Identifier: CA2965197069

Gene: SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80216971_80216972del , CM000679.2:g.80216971_80216972del	GRCh38
NC_000017.10:g.78190770_78190771del , CM000679.1:g.78190770_78190771del	GRCh37
NC_000017.9:g.75805365_75805366del	NCBI36
NG_008229.1:g.8430_8431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.249+61_249+62del MANE Select	ENSP00000314606.6:n.249+61_249+62del
ENST00000326317.10:c.249+61_249+62del	ENSP00000314606.6:n.249+61_249+62del
ENST00000570427.1:c.249+61_249+62del	ENSP00000459765.1:n.249+61_249+62del
ENST00000570923.1:c.284+61_284+62del	ENSP00000458200.1:n.284+61_284+62del
ENST00000571051.5:n.269+61_269+62del
ENST00000571075.1:n.330_331del
ENST00000571675.5:n.269+61_269+62del
ENST00000572208.5:n.267+61_267+62del
ENST00000573150.5:c.249+61_249+62del	ENSP00000459280.1:n.249+61_249+62del
ENST00000574505.5:c.194+61_194+62del
ENST00000575188.5:n.269+61_269+62del
ENST00000575282.5:n.258+61_258+62del
ENST00000576707.5:c.-13+61_-13+62del	ENSP00000461128.1:n.-13+61_-13+62del
ENST00000576941.5:c.249+61_249+62del	ENSP00000461160.1:n.249+61_249+62del
NM_000199.3:c.249+61_249+62del	NP_000190.1:n.249+61_249+62del
XM_005257582.2:c.249+61_249+62del	XP_005257639.1:n.249+61_249+62del
XM_005257583.3:c.249+61_249+62del	XP_005257640.1:n.249+61_249+62del
XM_011525126.1:c.249+61_249+62del	XP_011523428.1:n.249+61_249+62del
XM_011525127.1:c.249+61_249+62del	XP_011523429.1:n.249+61_249+62del
XR_934532.1:n.269+61_269+62del
NM_000199.4:c.249+61_249+62del	NP_000190.1:n.249+61_249+62del
NM_001352921.1:c.249+61_249+62del	NP_001339850.1:n.249+61_249+62del
NM_001352922.1:c.249+61_249+62del	NP_001339851.1:n.249+61_249+62del
NR_148201.1:n.336+61_336+62del
XM_005257583.4:c.249+61_249+62del	XP_005257640.1:n.249+61_249+62del
XM_017024952.1:c.249+61_249+62del	XP_016880441.1:n.249+61_249+62del
XR_001752585.1:n.269+61_269+62del
XR_001752586.1:n.269+61_269+62del
XR_001752587.1:n.269+61_269+62del
XR_001752588.1:n.269+61_269+62del
XR_001752589.1:n.269+61_269+62del
XR_001752590.1:n.269+61_269+62del
XR_001752591.1:n.269+61_269+62del
XR_001752592.1:n.269+61_269+62del
XR_002958057.1:n.269+61_269+62del
XR_934532.2:n.269+61_269+62del
NM_000199.5:c.249+61_249+62del MANE Select	NP_000190.1:n.249+61_249+62del
NM_001352921.2:c.249+61_249+62del	NP_001339850.1:n.249+61_249+62del
NM_001352922.2:c.249+61_249+62del	NP_001339851.1:n.249+61_249+62del
NR_148201.2:n.269+61_269+62del
NM_001352921.3:c.249+61_249+62del	NP_001339850.1:n.249+61_249+62del