Canonical Allele Identifier: CA387539514

Gene: SACS

Linked Data

• gnomAD v4: 13-23341572-A-C
• MyVariant Identifiers: chr13:g.23915711A>C (hg19) ; chr13:g.23341572A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341572A>C , CM000675.2:g.23341572A>C	GRCh38
NC_000013.10:g.23915711A>C , CM000675.1:g.23915711A>C	GRCh37
NC_000013.9:g.22813711A>C	NCBI36
NG_012342.1:g.97131T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12213T>G	ENSP00000508399.1:n.2185+12213T>G
ENST00000682944.1:c.2331T>G	ENSP00000507173.1:p.Asp777Glu
ENST00000683210.1:c.2185+12213T>G	ENSP00000506739.1:n.2185+12213T>G
ENST00000683270.1:c.2295T>G	ENSP00000507624.1:p.Asp765Glu
ENST00000683367.1:c.2177-12088T>G	ENSP00000507780.1:n.2177-12088T>G
ENST00000683489.1:c.2291+13T>G	ENSP00000508403.1:n.2291+13T>G
ENST00000683680.1:c.2318+13T>G	ENSP00000507223.1:n.2318+13T>G
ENST00000684163.1:c.2203+5239T>G	ENSP00000508262.1:n.2203+5239T>G
ENST00000684196.1:n.4543-12088T>G
ENST00000684325.1:c.2185+12213T>G	ENSP00000508121.1:n.2185+12213T>G
ENST00000684385.1:c.2220+5239T>G	ENSP00000507855.1:n.2220+5239T>G
ENST00000684497.1:c.2185+12213T>G	ENSP00000507057.1:n.2185+12213T>G
ENST00000382292.9:c.2304T>G MANE Select	ENSP00000371729.3:p.Asp768Glu
ENST00000423156.2:c.2186-12088T>G	ENSP00000390925.2:n.2186-12088T>G
ENST00000455470.6:c.2304T>G	ENSP00000406565.2:p.Asp768Glu
ENST00000382292.7:c.2304T>G	ENSP00000371729.3:p.Asp768Glu
ENST00000382298.7:c.2304T>G	ENSP00000371735.3:p.Asp768Glu
ENST00000402364.1:c.54T>G	ENSP00000385844.1:p.Asp18Glu
ENST00000423156.1:c.1058-12088T>G	ENSP00000390925.1:n.1058-12088T>G
ENST00000455470.5:c.2002T>G
NM_001278055.1:c.1863T>G	NP_001264984.1:p.Asp621Glu
NM_014363.5:c.2304T>G	NP_055178.3:p.Asp768Glu
XM_005266338.1:c.2331T>G	XP_005266395.1:p.Asp777Glu
XM_011535038.1:c.2355T>G	XP_011533340.1:p.Asp785Glu
XM_011535039.1:c.2322T>G	XP_011533341.1:p.Asp774Glu
XM_005266338.2:c.2331T>G	XP_005266395.1:p.Asp777Glu
XM_011535039.2:c.2322T>G	XP_011533341.1:p.Asp774Glu
XM_017020539.1:c.2295T>G	XP_016876028.1:p.Asp765Glu
XM_024449337.1:c.2331T>G	XP_024305105.1:p.Asp777Glu
NM_014363.6:c.2304T>G MANE Select	NP_055178.3:p.Asp768Glu
NM_001278055.2:c.1863T>G	NP_001264984.1:p.Asp621Glu