Canonical Allele Identifier: CA483159830

Gene: SACS

Linked Data

• ClinVar Variation Id: 1972254
• ClinVar RCV Id: RCV002750274
• MyVariant Identifiers: chr13:g.23908553G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334414G>C , CM000675.2:g.23334414G>C	GRCh38
NC_000013.10:g.23908553G>C , CM000675.1:g.23908553G>C	GRCh37
NC_000013.9:g.22806553G>C	NCBI36
NG_012342.1:g.104289C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19371C>G	ENSP00000508399.1:n.2185+19371C>G
ENST00000682944.1:c.9489C>G	ENSP00000507173.1:p.Pro3163=
ENST00000683210.1:c.2185+19371C>G	ENSP00000506739.1:n.2185+19371C>G
ENST00000683270.1:c.6445+3008C>G	ENSP00000507624.1:n.6445+3008C>G
ENST00000683367.1:c.2177-4930C>G	ENSP00000507780.1:n.2177-4930C>G
ENST00000683489.1:c.2292-4462C>G	ENSP00000508403.1:n.2292-4462C>G
ENST00000683680.1:c.2319-4462C>G	ENSP00000507223.1:n.2319-4462C>G
ENST00000684163.1:c.2204-4930C>G	ENSP00000508262.1:n.2204-4930C>G
ENST00000684196.1:n.4543-4930C>G
ENST00000684325.1:c.2186-12740C>G	ENSP00000508121.1:n.2186-12740C>G
ENST00000684385.1:c.2221-4930C>G	ENSP00000507855.1:n.2221-4930C>G
ENST00000684497.1:c.2186-11770C>G	ENSP00000507057.1:n.2186-11770C>G
ENST00000382292.9:c.9462C>G MANE Select	ENSP00000371729.3:p.Pro3154=
ENST00000423156.2:c.2186-4930C>G	ENSP00000390925.2:n.2186-4930C>G
ENST00000455470.6:c.2432-4930C>G	ENSP00000406565.2:n.2432-4930C>G
ENST00000382292.7:c.9462C>G	ENSP00000371729.3:p.Pro3154=
ENST00000382298.7:c.9462C>G	ENSP00000371735.3:p.Pro3154=
ENST00000402364.1:c.7212C>G	ENSP00000385844.1:p.Pro2404=
ENST00000423156.1:c.1058-4930C>G	ENSP00000390925.1:n.1058-4930C>G
ENST00000455470.5:c.2130-4930C>G
NM_001278055.1:c.9021C>G	NP_001264984.1:p.Pro3007=
NM_014363.5:c.9462C>G	NP_055178.3:p.Pro3154=
XM_005266338.1:c.9489C>G	XP_005266395.1:p.Pro3163=
XM_011535038.1:c.9513C>G	XP_011533340.1:p.Pro3171=
XM_011535039.1:c.9480C>G	XP_011533341.1:p.Pro3160=
XM_005266338.2:c.9489C>G	XP_005266395.1:p.Pro3163=
XM_011535039.2:c.9480C>G	XP_011533341.1:p.Pro3160=
XM_017020539.1:c.9453C>G	XP_016876028.1:p.Pro3151=
XM_024449337.1:c.9489C>G	XP_024305105.1:p.Pro3163=
NM_014363.6:c.9462C>G MANE Select	NP_055178.3:p.Pro3154=
NM_001278055.2:c.9021C>G	NP_001264984.1:p.Pro3007=