Canonical Allele Identifier: CA6911319

Gene: SACS

Linked Data

• ClinVar Variation Id: 1124825
• ClinVar RCV Id: RCV001456310 ; RCV001813824
• dbSNP Id: rs148824690
• ExAC: 13:23913060 T / C
• gnomAD v2: 13-23913060-T-C
• gnomAD v3: 13-23338921-T-C
• gnomAD v4: 13-23338921-T-C
• MyVariant Identifiers: chr13:g.23913060T>C (hg19) ; chr13:g.23338921T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23338921T>C , CM000675.2:g.23338921T>C	GRCh38
NC_000013.10:g.23913060T>C , CM000675.1:g.23913060T>C	GRCh37
NC_000013.9:g.22811060T>C	NCBI36
NG_012342.1:g.99782A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+14864A>G	ENSP00000508399.1:n.2185+14864A>G
ENST00000682944.1:c.4982A>G	ENSP00000507173.1:p.Gln1661Arg
ENST00000683210.1:c.2185+14864A>G	ENSP00000506739.1:n.2185+14864A>G
ENST00000683270.1:c.4946A>G	ENSP00000507624.1:p.Gln1649Arg
ENST00000683367.1:c.2177-9437A>G	ENSP00000507780.1:n.2177-9437A>G
ENST00000683489.1:c.2291+2664A>G	ENSP00000508403.1:n.2291+2664A>G
ENST00000683680.1:c.2318+2664A>G	ENSP00000507223.1:n.2318+2664A>G
ENST00000684163.1:c.2203+7890A>G	ENSP00000508262.1:n.2203+7890A>G
ENST00000684196.1:n.4543-9437A>G
ENST00000684325.1:c.2185+14864A>G	ENSP00000508121.1:n.2185+14864A>G
ENST00000684385.1:c.2220+7890A>G	ENSP00000507855.1:n.2220+7890A>G
ENST00000684497.1:c.2185+14864A>G	ENSP00000507057.1:n.2185+14864A>G
ENST00000382292.9:c.4955A>G MANE Select	ENSP00000371729.3:p.Gln1652Arg
ENST00000423156.2:c.2186-9437A>G	ENSP00000390925.2:n.2186-9437A>G
ENST00000455470.6:c.2431+2524A>G	ENSP00000406565.2:n.2431+2524A>G
ENST00000382292.7:c.4955A>G	ENSP00000371729.3:p.Gln1652Arg
ENST00000382298.7:c.4955A>G	ENSP00000371735.3:p.Gln1652Arg
ENST00000402364.1:c.2705A>G	ENSP00000385844.1:p.Gln902Arg
ENST00000423156.1:c.1058-9437A>G	ENSP00000390925.1:n.1058-9437A>G
ENST00000455470.5:c.2129+2524A>G
NM_001278055.1:c.4514A>G	NP_001264984.1:p.Gln1505Arg
NM_014363.5:c.4955A>G	NP_055178.3:p.Gln1652Arg
XM_005266338.1:c.4982A>G	XP_005266395.1:p.Gln1661Arg
XM_011535038.1:c.5006A>G	XP_011533340.1:p.Gln1669Arg
XM_011535039.1:c.4973A>G	XP_011533341.1:p.Gln1658Arg
XM_005266338.2:c.4982A>G	XP_005266395.1:p.Gln1661Arg
XM_011535039.2:c.4973A>G	XP_011533341.1:p.Gln1658Arg
XM_017020539.1:c.4946A>G	XP_016876028.1:p.Gln1649Arg
XM_024449337.1:c.4982A>G	XP_024305105.1:p.Gln1661Arg
NM_014363.6:c.4955A>G MANE Select	NP_055178.3:p.Gln1652Arg
NM_001278055.2:c.4514A>G	NP_001264984.1:p.Gln1505Arg