Canonical Allele Identifier: CA387536898

Gene: SACS

Linked Data

• COSMIC: COSM1513931 ; COSM1513932
• MyVariant Identifiers: chr13:g.23914963C>G (hg19) ; chr13:g.23340824C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23340824C>G , CM000675.2:g.23340824C>G	GRCh38
NC_000013.10:g.23914963C>G , CM000675.1:g.23914963C>G	GRCh37
NC_000013.9:g.22812963C>G	NCBI36
NG_012342.1:g.97879G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+12961G>C	ENSP00000508399.1:n.2185+12961G>C
ENST00000682944.1:c.3079G>C	ENSP00000507173.1:p.Glu1027Gln
ENST00000683210.1:c.2185+12961G>C	ENSP00000506739.1:n.2185+12961G>C
ENST00000683270.1:c.3043G>C	ENSP00000507624.1:p.Glu1015Gln
ENST00000683367.1:c.2177-11340G>C	ENSP00000507780.1:n.2177-11340G>C
ENST00000683489.1:c.2291+761G>C	ENSP00000508403.1:n.2291+761G>C
ENST00000683680.1:c.2318+761G>C	ENSP00000507223.1:n.2318+761G>C
ENST00000684163.1:c.2203+5987G>C	ENSP00000508262.1:n.2203+5987G>C
ENST00000684196.1:n.4543-11340G>C
ENST00000684325.1:c.2185+12961G>C	ENSP00000508121.1:n.2185+12961G>C
ENST00000684385.1:c.2220+5987G>C	ENSP00000507855.1:n.2220+5987G>C
ENST00000684497.1:c.2185+12961G>C	ENSP00000507057.1:n.2185+12961G>C
ENST00000382292.9:c.3052G>C MANE Select	ENSP00000371729.3:p.Glu1018Gln
ENST00000423156.2:c.2186-11340G>C	ENSP00000390925.2:n.2186-11340G>C
ENST00000455470.6:c.2431+621G>C	ENSP00000406565.2:n.2431+621G>C
ENST00000382292.7:c.3052G>C	ENSP00000371729.3:p.Glu1018Gln
ENST00000382298.7:c.3052G>C	ENSP00000371735.3:p.Glu1018Gln
ENST00000402364.1:c.802G>C	ENSP00000385844.1:p.Glu268Gln
ENST00000423156.1:c.1058-11340G>C	ENSP00000390925.1:n.1058-11340G>C
ENST00000455470.5:c.2129+621G>C
NM_001278055.1:c.2611G>C	NP_001264984.1:p.Glu871Gln
NM_014363.5:c.3052G>C	NP_055178.3:p.Glu1018Gln
XM_005266338.1:c.3079G>C	XP_005266395.1:p.Glu1027Gln
XM_011535038.1:c.3103G>C	XP_011533340.1:p.Glu1035Gln
XM_011535039.1:c.3070G>C	XP_011533341.1:p.Glu1024Gln
XM_005266338.2:c.3079G>C	XP_005266395.1:p.Glu1027Gln
XM_011535039.2:c.3070G>C	XP_011533341.1:p.Glu1024Gln
XM_017020539.1:c.3043G>C	XP_016876028.1:p.Glu1015Gln
XM_024449337.1:c.3079G>C	XP_024305105.1:p.Glu1027Gln
NM_014363.6:c.3052G>C MANE Select	NP_055178.3:p.Glu1018Gln
NM_001278055.2:c.2611G>C	NP_001264984.1:p.Glu871Gln