Canonical Allele Identifier: CA16041604

Gene: SACS

Linked Data

• ClinVar Variation Id: 370549
• ClinVar RCV Id: RCV000412194
• dbSNP Id: rs1057516578
• COSMIC: COSM5563634 ; COSM5563635
• MyVariant Identifiers: chr13:g.23907151G>A (hg19) ; chr13:g.23333012G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333012G>A , CM000675.2:g.23333012G>A	GRCh38
NC_000013.10:g.23907151G>A , CM000675.1:g.23907151G>A	GRCh37
NC_000013.9:g.22805151G>A	NCBI36
NG_012342.1:g.105691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20773C>T	ENSP00000508399.1:n.2185+20773C>T
ENST00000682944.1:c.10891C>T	ENSP00000507173.1:p.Gln3631Ter
ENST00000683210.1:c.2185+20773C>T	ENSP00000506739.1:n.2185+20773C>T
ENST00000683270.1:c.6446-3528C>T	ENSP00000507624.1:n.6446-3528C>T
ENST00000683367.1:c.2177-3528C>T	ENSP00000507780.1:n.2177-3528C>T
ENST00000683489.1:c.2292-3060C>T	ENSP00000508403.1:n.2292-3060C>T
ENST00000683680.1:c.2319-3060C>T	ENSP00000507223.1:n.2319-3060C>T
ENST00000684163.1:c.2204-3528C>T	ENSP00000508262.1:n.2204-3528C>T
ENST00000684196.1:n.4543-3528C>T
ENST00000684325.1:c.2186-11338C>T	ENSP00000508121.1:n.2186-11338C>T
ENST00000684385.1:c.2221-3528C>T	ENSP00000507855.1:n.2221-3528C>T
ENST00000684497.1:c.2186-10368C>T	ENSP00000507057.1:n.2186-10368C>T
ENST00000382292.9:c.10864C>T MANE Select	ENSP00000371729.3:p.Gln3622Ter
ENST00000423156.2:c.2186-3528C>T	ENSP00000390925.2:n.2186-3528C>T
ENST00000455470.6:c.2432-3528C>T	ENSP00000406565.2:n.2432-3528C>T
ENST00000382292.7:c.10864C>T	ENSP00000371729.3:p.Gln3622Ter
ENST00000382298.7:c.10864C>T	ENSP00000371735.3:p.Gln3622Ter
ENST00000402364.1:c.8614C>T	ENSP00000385844.1:p.Gln2872Ter
ENST00000423156.1:c.1058-3528C>T	ENSP00000390925.1:n.1058-3528C>T
ENST00000455470.5:c.2130-3528C>T
NM_001278055.1:c.10423C>T	NP_001264984.1:p.Gln3475Ter
NM_014363.5:c.10864C>T	NP_055178.3:p.Gln3622Ter
XM_005266338.1:c.10891C>T	XP_005266395.1:p.Gln3631Ter
XM_011535038.1:c.10915C>T	XP_011533340.1:p.Gln3639Ter
XM_011535039.1:c.10882C>T	XP_011533341.1:p.Gln3628Ter
XM_005266338.2:c.10891C>T	XP_005266395.1:p.Gln3631Ter
XM_011535039.2:c.10882C>T	XP_011533341.1:p.Gln3628Ter
XM_017020539.1:c.10855C>T	XP_016876028.1:p.Gln3619Ter
XM_024449337.1:c.10891C>T	XP_024305105.1:p.Gln3631Ter
NM_014363.6:c.10864C>T MANE Select	NP_055178.3:p.Gln3622Ter
NM_001278055.2:c.10423C>T	NP_001264984.1:p.Gln3475Ter