Canonical Allele Identifier: CA387518069

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23910178C>G (hg19) ; chr13:g.23336039C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336039C>G , CM000675.2:g.23336039C>G	GRCh38
NC_000013.10:g.23910178C>G , CM000675.1:g.23910178C>G	GRCh37
NC_000013.9:g.22808178C>G	NCBI36
NG_012342.1:g.102664G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17746G>C	ENSP00000508399.1:n.2185+17746G>C
ENST00000682944.1:c.7864G>C	ENSP00000507173.1:p.Glu2622Gln
ENST00000683210.1:c.2185+17746G>C	ENSP00000506739.1:n.2185+17746G>C
ENST00000683270.1:c.6445+1383G>C	ENSP00000507624.1:n.6445+1383G>C
ENST00000683367.1:c.2177-6555G>C	ENSP00000507780.1:n.2177-6555G>C
ENST00000683489.1:c.2291+5546G>C	ENSP00000508403.1:n.2291+5546G>C
ENST00000683680.1:c.2318+5546G>C	ENSP00000507223.1:n.2318+5546G>C
ENST00000684163.1:c.2204-6555G>C	ENSP00000508262.1:n.2204-6555G>C
ENST00000684196.1:n.4543-6555G>C
ENST00000684325.1:c.2186-14365G>C	ENSP00000508121.1:n.2186-14365G>C
ENST00000684385.1:c.2221-6555G>C	ENSP00000507855.1:n.2221-6555G>C
ENST00000684497.1:c.2186-13395G>C	ENSP00000507057.1:n.2186-13395G>C
ENST00000382292.9:c.7837G>C MANE Select	ENSP00000371729.3:p.Glu2613Gln
ENST00000423156.2:c.2186-6555G>C	ENSP00000390925.2:n.2186-6555G>C
ENST00000455470.6:c.2431+5406G>C	ENSP00000406565.2:n.2431+5406G>C
ENST00000382292.7:c.7837G>C	ENSP00000371729.3:p.Glu2613Gln
ENST00000382298.7:c.7837G>C	ENSP00000371735.3:p.Glu2613Gln
ENST00000402364.1:c.5587G>C	ENSP00000385844.1:p.Glu1863Gln
ENST00000423156.1:c.1058-6555G>C	ENSP00000390925.1:n.1058-6555G>C
ENST00000455470.5:c.2129+5406G>C
NM_001278055.1:c.7396G>C	NP_001264984.1:p.Glu2466Gln
NM_014363.5:c.7837G>C	NP_055178.3:p.Glu2613Gln
XM_005266338.1:c.7864G>C	XP_005266395.1:p.Glu2622Gln
XM_011535038.1:c.7888G>C	XP_011533340.1:p.Glu2630Gln
XM_011535039.1:c.7855G>C	XP_011533341.1:p.Glu2619Gln
XM_005266338.2:c.7864G>C	XP_005266395.1:p.Glu2622Gln
XM_011535039.2:c.7855G>C	XP_011533341.1:p.Glu2619Gln
XM_017020539.1:c.7828G>C	XP_016876028.1:p.Glu2610Gln
XM_024449337.1:c.7864G>C	XP_024305105.1:p.Glu2622Gln
NM_014363.6:c.7837G>C MANE Select	NP_055178.3:p.Glu2613Gln
NM_001278055.2:c.7396G>C	NP_001264984.1:p.Glu2466Gln