Canonical Allele Identifier: CA483158322

Gene: SACS

Linked Data

• dbSNP Id: rs1883462785
• MyVariant Identifiers: chr13:g.23905472A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23331333A>G , CM000675.2:g.23331333A>G	GRCh38
NC_000013.10:g.23905472A>G , CM000675.1:g.23905472A>G	GRCh37
NC_000013.9:g.22803472A>G	NCBI36
NG_012342.1:g.107370T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-19218T>C	ENSP00000508399.1:n.2186-19218T>C
ENST00000682944.1:c.12570T>C	ENSP00000507173.1:p.Tyr4190=
ENST00000683210.1:c.2185+22452T>C	ENSP00000506739.1:n.2185+22452T>C
ENST00000683270.1:c.6446-1849T>C	ENSP00000507624.1:n.6446-1849T>C
ENST00000683367.1:c.2177-1849T>C	ENSP00000507780.1:n.2177-1849T>C
ENST00000683489.1:c.2292-1381T>C	ENSP00000508403.1:n.2292-1381T>C
ENST00000683680.1:c.2319-1381T>C	ENSP00000507223.1:n.2319-1381T>C
ENST00000684163.1:c.2204-1849T>C	ENSP00000508262.1:n.2204-1849T>C
ENST00000684196.1:n.4543-1849T>C
ENST00000684325.1:c.2186-9659T>C	ENSP00000508121.1:n.2186-9659T>C
ENST00000684385.1:c.2221-1849T>C	ENSP00000507855.1:n.2221-1849T>C
ENST00000684497.1:c.2186-8689T>C	ENSP00000507057.1:n.2186-8689T>C
ENST00000382292.9:c.12543T>C MANE Select	ENSP00000371729.3:p.Tyr4181=
ENST00000423156.2:c.2186-1849T>C	ENSP00000390925.2:n.2186-1849T>C
ENST00000455470.6:c.2432-1849T>C	ENSP00000406565.2:n.2432-1849T>C
ENST00000382292.7:c.12543T>C	ENSP00000371729.3:p.Tyr4181=
ENST00000382298.7:c.12543T>C	ENSP00000371735.3:p.Tyr4181=
ENST00000402364.1:c.10293T>C	ENSP00000385844.1:p.Tyr3431=
ENST00000423156.1:c.1058-1849T>C	ENSP00000390925.1:n.1058-1849T>C
ENST00000455470.5:c.2130-1849T>C
NM_001278055.1:c.12102T>C	NP_001264984.1:p.Tyr4034=
NM_014363.5:c.12543T>C	NP_055178.3:p.Tyr4181=
XM_005266338.1:c.12570T>C	XP_005266395.1:p.Tyr4190=
XM_011535038.1:c.12594T>C	XP_011533340.1:p.Tyr4198=
XM_011535039.1:c.12561T>C	XP_011533341.1:p.Tyr4187=
XM_005266338.2:c.12570T>C	XP_005266395.1:p.Tyr4190=
XM_011535039.2:c.12561T>C	XP_011533341.1:p.Tyr4187=
XM_017020539.1:c.12534T>C	XP_016876028.1:p.Tyr4178=
XM_024449337.1:c.12570T>C	XP_024305105.1:p.Tyr4190=
NM_014363.6:c.12543T>C MANE Select	NP_055178.3:p.Tyr4181=
NM_001278055.2:c.12102T>C	NP_001264984.1:p.Tyr4034=