Canonical Allele Identifier: CA387538262

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23915339T>C (hg19) ; chr13:g.23341200T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341200T>C , CM000675.2:g.23341200T>C	GRCh38
NC_000013.10:g.23915339T>C , CM000675.1:g.23915339T>C	GRCh37
NC_000013.9:g.22813339T>C	NCBI36
NG_012342.1:g.97503A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12585A>G	ENSP00000508399.1:n.2185+12585A>G
ENST00000682944.1:c.2703A>G	ENSP00000507173.1:p.Ile901Met
ENST00000683210.1:c.2185+12585A>G	ENSP00000506739.1:n.2185+12585A>G
ENST00000683270.1:c.2667A>G	ENSP00000507624.1:p.Ile889Met
ENST00000683367.1:c.2177-11716A>G	ENSP00000507780.1:n.2177-11716A>G
ENST00000683489.1:c.2291+385A>G	ENSP00000508403.1:n.2291+385A>G
ENST00000683680.1:c.2318+385A>G	ENSP00000507223.1:n.2318+385A>G
ENST00000684163.1:c.2203+5611A>G	ENSP00000508262.1:n.2203+5611A>G
ENST00000684196.1:n.4543-11716A>G
ENST00000684325.1:c.2185+12585A>G	ENSP00000508121.1:n.2185+12585A>G
ENST00000684385.1:c.2220+5611A>G	ENSP00000507855.1:n.2220+5611A>G
ENST00000684497.1:c.2185+12585A>G	ENSP00000507057.1:n.2185+12585A>G
ENST00000382292.9:c.2676A>G MANE Select	ENSP00000371729.3:p.Ile892Met
ENST00000423156.2:c.2186-11716A>G	ENSP00000390925.2:n.2186-11716A>G
ENST00000455470.6:c.2431+245A>G	ENSP00000406565.2:n.2431+245A>G
ENST00000382292.7:c.2676A>G	ENSP00000371729.3:p.Ile892Met
ENST00000382298.7:c.2676A>G	ENSP00000371735.3:p.Ile892Met
ENST00000402364.1:c.426A>G	ENSP00000385844.1:p.Ile142Met
ENST00000423156.1:c.1058-11716A>G	ENSP00000390925.1:n.1058-11716A>G
ENST00000455470.5:c.2129+245A>G
NM_001278055.1:c.2235A>G	NP_001264984.1:p.Ile745Met
NM_014363.5:c.2676A>G	NP_055178.3:p.Ile892Met
XM_005266338.1:c.2703A>G	XP_005266395.1:p.Ile901Met
XM_011535038.1:c.2727A>G	XP_011533340.1:p.Ile909Met
XM_011535039.1:c.2694A>G	XP_011533341.1:p.Ile898Met
XM_005266338.2:c.2703A>G	XP_005266395.1:p.Ile901Met
XM_011535039.2:c.2694A>G	XP_011533341.1:p.Ile898Met
XM_017020539.1:c.2667A>G	XP_016876028.1:p.Ile889Met
XM_024449337.1:c.2703A>G	XP_024305105.1:p.Ile901Met
NM_014363.6:c.2676A>G MANE Select	NP_055178.3:p.Ile892Met
NM_001278055.2:c.2235A>G	NP_001264984.1:p.Ile745Met