Canonical Allele Identifier: CA387506211

Gene: SACS

Linked Data

• ClinVar Variation Id: 527992
• ClinVar RCV Id: RCV000633036
• dbSNP Id: rs1555249362
• MyVariant Identifiers: chr13:g.23905006G>C (hg19) ; chr13:g.23330867G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330867G>C , CM000675.2:g.23330867G>C	GRCh38
NC_000013.10:g.23905006G>C , CM000675.1:g.23905006G>C	GRCh37
NC_000013.9:g.22803006G>C	NCBI36
NG_012342.1:g.107836C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-18752C>G	ENSP00000508399.1:n.2186-18752C>G
ENST00000682944.1:c.13036C>G	ENSP00000507173.1:p.His4346Asp
ENST00000683210.1:c.2185+22918C>G	ENSP00000506739.1:n.2185+22918C>G
ENST00000683270.1:c.6446-1383C>G	ENSP00000507624.1:n.6446-1383C>G
ENST00000683367.1:c.2177-1383C>G	ENSP00000507780.1:n.2177-1383C>G
ENST00000683489.1:c.2292-915C>G	ENSP00000508403.1:n.2292-915C>G
ENST00000683680.1:c.2319-915C>G	ENSP00000507223.1:n.2319-915C>G
ENST00000684163.1:c.2204-1383C>G	ENSP00000508262.1:n.2204-1383C>G
ENST00000684196.1:n.4543-1383C>G
ENST00000684325.1:c.2186-9193C>G	ENSP00000508121.1:n.2186-9193C>G
ENST00000684385.1:c.2221-1383C>G	ENSP00000507855.1:n.2221-1383C>G
ENST00000684497.1:c.2186-8223C>G	ENSP00000507057.1:n.2186-8223C>G
ENST00000382292.9:c.13009C>G MANE Select	ENSP00000371729.3:p.His4337Asp
ENST00000423156.2:c.2186-1383C>G	ENSP00000390925.2:n.2186-1383C>G
ENST00000455470.6:c.2432-1383C>G	ENSP00000406565.2:n.2432-1383C>G
ENST00000382292.7:c.13009C>G	ENSP00000371729.3:p.His4337Asp
ENST00000382298.7:c.13009C>G	ENSP00000371735.3:p.His4337Asp
ENST00000402364.1:c.10759C>G	ENSP00000385844.1:p.His3587Asp
ENST00000423156.1:c.1058-1383C>G	ENSP00000390925.1:n.1058-1383C>G
ENST00000455470.5:c.2130-1383C>G
NM_001278055.1:c.12568C>G	NP_001264984.1:p.His4190Asp
NM_014363.5:c.13009C>G	NP_055178.3:p.His4337Asp
XM_005266338.1:c.13036C>G	XP_005266395.1:p.His4346Asp
XM_011535038.1:c.13060C>G	XP_011533340.1:p.His4354Asp
XM_011535039.1:c.13027C>G	XP_011533341.1:p.His4343Asp
XM_005266338.2:c.13036C>G	XP_005266395.1:p.His4346Asp
XM_011535039.2:c.13027C>G	XP_011533341.1:p.His4343Asp
XM_017020539.1:c.13000C>G	XP_016876028.1:p.His4334Asp
XM_024449337.1:c.13036C>G	XP_024305105.1:p.His4346Asp
NM_014363.6:c.13009C>G MANE Select	NP_055178.3:p.His4337Asp
NM_001278055.2:c.12568C>G	NP_001264984.1:p.His4190Asp