Canonical Allele Identifier: CA387514454

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23908585C>G (hg19) ; chr13:g.23334446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334446C>G , CM000675.2:g.23334446C>G	GRCh38
NC_000013.10:g.23908585C>G , CM000675.1:g.23908585C>G	GRCh37
NC_000013.9:g.22806585C>G	NCBI36
NG_012342.1:g.104257G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19339G>C	ENSP00000508399.1:n.2185+19339G>C
ENST00000682944.1:c.9457G>C	ENSP00000507173.1:p.Glu3153Gln
ENST00000683210.1:c.2185+19339G>C	ENSP00000506739.1:n.2185+19339G>C
ENST00000683270.1:c.6445+2976G>C	ENSP00000507624.1:n.6445+2976G>C
ENST00000683367.1:c.2177-4962G>C	ENSP00000507780.1:n.2177-4962G>C
ENST00000683489.1:c.2292-4494G>C	ENSP00000508403.1:n.2292-4494G>C
ENST00000683680.1:c.2319-4494G>C	ENSP00000507223.1:n.2319-4494G>C
ENST00000684163.1:c.2204-4962G>C	ENSP00000508262.1:n.2204-4962G>C
ENST00000684196.1:n.4543-4962G>C
ENST00000684325.1:c.2186-12772G>C	ENSP00000508121.1:n.2186-12772G>C
ENST00000684385.1:c.2221-4962G>C	ENSP00000507855.1:n.2221-4962G>C
ENST00000684497.1:c.2186-11802G>C	ENSP00000507057.1:n.2186-11802G>C
ENST00000382292.9:c.9430G>C MANE Select	ENSP00000371729.3:p.Glu3144Gln
ENST00000423156.2:c.2186-4962G>C	ENSP00000390925.2:n.2186-4962G>C
ENST00000455470.6:c.2432-4962G>C	ENSP00000406565.2:n.2432-4962G>C
ENST00000382292.7:c.9430G>C	ENSP00000371729.3:p.Glu3144Gln
ENST00000382298.7:c.9430G>C	ENSP00000371735.3:p.Glu3144Gln
ENST00000402364.1:c.7180G>C	ENSP00000385844.1:p.Glu2394Gln
ENST00000423156.1:c.1058-4962G>C	ENSP00000390925.1:n.1058-4962G>C
ENST00000455470.5:c.2130-4962G>C
NM_001278055.1:c.8989G>C	NP_001264984.1:p.Glu2997Gln
NM_014363.5:c.9430G>C	NP_055178.3:p.Glu3144Gln
XM_005266338.1:c.9457G>C	XP_005266395.1:p.Glu3153Gln
XM_011535038.1:c.9481G>C	XP_011533340.1:p.Glu3161Gln
XM_011535039.1:c.9448G>C	XP_011533341.1:p.Glu3150Gln
XM_005266338.2:c.9457G>C	XP_005266395.1:p.Glu3153Gln
XM_011535039.2:c.9448G>C	XP_011533341.1:p.Glu3150Gln
XM_017020539.1:c.9421G>C	XP_016876028.1:p.Glu3141Gln
XM_024449337.1:c.9457G>C	XP_024305105.1:p.Glu3153Gln
NM_014363.6:c.9430G>C MANE Select	NP_055178.3:p.Glu3144Gln
NM_001278055.2:c.8989G>C	NP_001264984.1:p.Glu2997Gln