Canonical Allele Identifier: CA483162342

Gene: SACS

Linked Data

• ClinVar Variation Id: 2860232
• ClinVar RCV Id: RCV003752457
• MyVariant Identifiers: chr13:g.23913077C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23338938C>A , CM000675.2:g.23338938C>A	GRCh38
NC_000013.10:g.23913077C>A , CM000675.1:g.23913077C>A	GRCh37
NC_000013.9:g.22811077C>A	NCBI36
NG_012342.1:g.99765G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+14847G>T	ENSP00000508399.1:n.2185+14847G>T
ENST00000682944.1:c.4965G>T	ENSP00000507173.1:p.Leu1655=
ENST00000683210.1:c.2185+14847G>T	ENSP00000506739.1:n.2185+14847G>T
ENST00000683270.1:c.4929G>T	ENSP00000507624.1:p.Leu1643=
ENST00000683367.1:c.2177-9454G>T	ENSP00000507780.1:n.2177-9454G>T
ENST00000683489.1:c.2291+2647G>T	ENSP00000508403.1:n.2291+2647G>T
ENST00000683680.1:c.2318+2647G>T	ENSP00000507223.1:n.2318+2647G>T
ENST00000684163.1:c.2203+7873G>T	ENSP00000508262.1:n.2203+7873G>T
ENST00000684196.1:n.4543-9454G>T
ENST00000684325.1:c.2185+14847G>T	ENSP00000508121.1:n.2185+14847G>T
ENST00000684385.1:c.2220+7873G>T	ENSP00000507855.1:n.2220+7873G>T
ENST00000684497.1:c.2185+14847G>T	ENSP00000507057.1:n.2185+14847G>T
ENST00000382292.9:c.4938G>T MANE Select	ENSP00000371729.3:p.Leu1646=
ENST00000423156.2:c.2186-9454G>T	ENSP00000390925.2:n.2186-9454G>T
ENST00000455470.6:c.2431+2507G>T	ENSP00000406565.2:n.2431+2507G>T
ENST00000382292.7:c.4938G>T	ENSP00000371729.3:p.Leu1646=
ENST00000382298.7:c.4938G>T	ENSP00000371735.3:p.Leu1646=
ENST00000402364.1:c.2688G>T	ENSP00000385844.1:p.Leu896=
ENST00000423156.1:c.1058-9454G>T	ENSP00000390925.1:n.1058-9454G>T
ENST00000455470.5:c.2129+2507G>T
NM_001278055.1:c.4497G>T	NP_001264984.1:p.Leu1499=
NM_014363.5:c.4938G>T	NP_055178.3:p.Leu1646=
XM_005266338.1:c.4965G>T	XP_005266395.1:p.Leu1655=
XM_011535038.1:c.4989G>T	XP_011533340.1:p.Leu1663=
XM_011535039.1:c.4956G>T	XP_011533341.1:p.Leu1652=
XM_005266338.2:c.4965G>T	XP_005266395.1:p.Leu1655=
XM_011535039.2:c.4956G>T	XP_011533341.1:p.Leu1652=
XM_017020539.1:c.4929G>T	XP_016876028.1:p.Leu1643=
XM_024449337.1:c.4965G>T	XP_024305105.1:p.Leu1655=
NM_014363.6:c.4938G>T MANE Select	NP_055178.3:p.Leu1646=
NM_001278055.2:c.4497G>T	NP_001264984.1:p.Leu1499=