Canonical Allele Identifier: CA387523568

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911766T>A (hg19) ; chr13:g.23337627T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337627T>A , CM000675.2:g.23337627T>A	GRCh38
NC_000013.10:g.23911766T>A , CM000675.1:g.23911766T>A	GRCh37
NC_000013.9:g.22809766T>A	NCBI36
NG_012342.1:g.101076A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+16158A>T	ENSP00000508399.1:n.2185+16158A>T
ENST00000682944.1:c.6276A>T	ENSP00000507173.1:p.Glu2092Asp
ENST00000683210.1:c.2185+16158A>T	ENSP00000506739.1:n.2185+16158A>T
ENST00000683270.1:c.6240A>T	ENSP00000507624.1:p.Glu2080Asp
ENST00000683367.1:c.2177-8143A>T	ENSP00000507780.1:n.2177-8143A>T
ENST00000683489.1:c.2291+3958A>T	ENSP00000508403.1:n.2291+3958A>T
ENST00000683680.1:c.2318+3958A>T	ENSP00000507223.1:n.2318+3958A>T
ENST00000684163.1:c.2204-8143A>T	ENSP00000508262.1:n.2204-8143A>T
ENST00000684196.1:n.4543-8143A>T
ENST00000684325.1:c.2186-15953A>T	ENSP00000508121.1:n.2186-15953A>T
ENST00000684385.1:c.2221-8143A>T	ENSP00000507855.1:n.2221-8143A>T
ENST00000684497.1:c.2186-14983A>T	ENSP00000507057.1:n.2186-14983A>T
ENST00000382292.9:c.6249A>T MANE Select	ENSP00000371729.3:p.Glu2083Asp
ENST00000423156.2:c.2186-8143A>T	ENSP00000390925.2:n.2186-8143A>T
ENST00000455470.6:c.2431+3818A>T	ENSP00000406565.2:n.2431+3818A>T
ENST00000382292.7:c.6249A>T	ENSP00000371729.3:p.Glu2083Asp
ENST00000382298.7:c.6249A>T	ENSP00000371735.3:p.Glu2083Asp
ENST00000402364.1:c.3999A>T	ENSP00000385844.1:p.Glu1333Asp
ENST00000423156.1:c.1058-8143A>T	ENSP00000390925.1:n.1058-8143A>T
ENST00000455470.5:c.2129+3818A>T
NM_001278055.1:c.5808A>T	NP_001264984.1:p.Glu1936Asp
NM_014363.5:c.6249A>T	NP_055178.3:p.Glu2083Asp
XM_005266338.1:c.6276A>T	XP_005266395.1:p.Glu2092Asp
XM_011535038.1:c.6300A>T	XP_011533340.1:p.Glu2100Asp
XM_011535039.1:c.6267A>T	XP_011533341.1:p.Glu2089Asp
XM_005266338.2:c.6276A>T	XP_005266395.1:p.Glu2092Asp
XM_011535039.2:c.6267A>T	XP_011533341.1:p.Glu2089Asp
XM_017020539.1:c.6240A>T	XP_016876028.1:p.Glu2080Asp
XM_024449337.1:c.6276A>T	XP_024305105.1:p.Glu2092Asp
NM_014363.6:c.6249A>T MANE Select	NP_055178.3:p.Glu2083Asp
NM_001278055.2:c.5808A>T	NP_001264984.1:p.Glu1936Asp