Canonical Allele Identifier: CA401364237

Gene: SGSH

Linked Data

• MyVariant Identifiers: chr17:g.78190879G>C (hg19) ; chr17:g.80217080G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80217080G>C , CM000679.2:g.80217080G>C	GRCh38
NC_000017.10:g.78190879G>C , CM000679.1:g.78190879G>C	GRCh37
NC_000017.9:g.75805474G>C	NCBI36
NG_008229.1:g.8321C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326317.11:c.201C>G MANE Select	ENSP00000314606.6:p.Val67=
ENST00000326317.10:c.201C>G	ENSP00000314606.6:p.Val67=
ENST00000570427.1:c.201C>G	ENSP00000459765.1:p.Val67=
ENST00000570923.1:c.236C>G	ENSP00000458200.1:p.Ser79Ter
ENST00000571051.5:n.221C>G
ENST00000571075.1:n.221C>G
ENST00000571675.5:n.221C>G
ENST00000572208.5:n.219C>G
ENST00000573150.5:c.201C>G	ENSP00000459280.1:p.Val67=
ENST00000574505.5:c.146C>G
ENST00000575188.5:n.221C>G
ENST00000575282.5:n.210C>G
ENST00000576707.5:c.-61C>G	ENSP00000461128.1:n.-61C>G
ENST00000576941.5:c.201C>G	ENSP00000461160.1:p.Val67=
NM_000199.3:c.201C>G	NP_000190.1:p.Val67=
XM_005257582.2:c.201C>G	XP_005257639.1:p.Val67=
XM_005257583.3:c.201C>G	XP_005257640.1:p.Val67=
XM_011525126.1:c.201C>G	XP_011523428.1:p.Val67=
XM_011525127.1:c.201C>G	XP_011523429.1:p.Val67=
XR_934532.1:n.221C>G
NM_000199.4:c.201C>G	NP_000190.1:p.Val67=
NM_001352921.1:c.201C>G	NP_001339850.1:p.Val67=
NM_001352922.1:c.201C>G	NP_001339851.1:p.Val67=
NR_148201.1:n.288C>G
XM_005257583.4:c.201C>G	XP_005257640.1:p.Val67=
XM_017024952.1:c.201C>G	XP_016880441.1:p.Val67=
XR_001752585.1:n.221C>G
XR_001752586.1:n.221C>G
XR_001752587.1:n.221C>G
XR_001752588.1:n.221C>G
XR_001752589.1:n.221C>G
XR_001752590.1:n.221C>G
XR_001752591.1:n.221C>G
XR_001752592.1:n.221C>G
XR_002958057.1:n.221C>G
XR_934532.2:n.221C>G
NM_000199.5:c.201C>G MANE Select	NP_000190.1:p.Val67=
NM_001352921.2:c.201C>G	NP_001339850.1:p.Val67=
NM_001352922.2:c.201C>G	NP_001339851.1:p.Val67=
NR_148201.2:n.221C>G
NM_001352921.3:c.201C>G	NP_001339850.1:p.Val67=