Canonical Allele Identifier: CA387518207

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23910215A>C (hg19) ; chr13:g.23336076A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336076A>C , CM000675.2:g.23336076A>C	GRCh38
NC_000013.10:g.23910215A>C , CM000675.1:g.23910215A>C	GRCh37
NC_000013.9:g.22808215A>C	NCBI36
NG_012342.1:g.102627T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17709T>G	ENSP00000508399.1:n.2185+17709T>G
ENST00000682944.1:c.7827T>G	ENSP00000507173.1:p.Asp2609Glu
ENST00000683210.1:c.2185+17709T>G	ENSP00000506739.1:n.2185+17709T>G
ENST00000683270.1:c.6445+1346T>G	ENSP00000507624.1:n.6445+1346T>G
ENST00000683367.1:c.2177-6592T>G	ENSP00000507780.1:n.2177-6592T>G
ENST00000683489.1:c.2291+5509T>G	ENSP00000508403.1:n.2291+5509T>G
ENST00000683680.1:c.2318+5509T>G	ENSP00000507223.1:n.2318+5509T>G
ENST00000684163.1:c.2204-6592T>G	ENSP00000508262.1:n.2204-6592T>G
ENST00000684196.1:n.4543-6592T>G
ENST00000684325.1:c.2186-14402T>G	ENSP00000508121.1:n.2186-14402T>G
ENST00000684385.1:c.2221-6592T>G	ENSP00000507855.1:n.2221-6592T>G
ENST00000684497.1:c.2186-13432T>G	ENSP00000507057.1:n.2186-13432T>G
ENST00000382292.9:c.7800T>G MANE Select	ENSP00000371729.3:p.Asp2600Glu
ENST00000423156.2:c.2186-6592T>G	ENSP00000390925.2:n.2186-6592T>G
ENST00000455470.6:c.2431+5369T>G	ENSP00000406565.2:n.2431+5369T>G
ENST00000382292.7:c.7800T>G	ENSP00000371729.3:p.Asp2600Glu
ENST00000382298.7:c.7800T>G	ENSP00000371735.3:p.Asp2600Glu
ENST00000402364.1:c.5550T>G	ENSP00000385844.1:p.Asp1850Glu
ENST00000423156.1:c.1058-6592T>G	ENSP00000390925.1:n.1058-6592T>G
ENST00000455470.5:c.2129+5369T>G
NM_001278055.1:c.7359T>G	NP_001264984.1:p.Asp2453Glu
NM_014363.5:c.7800T>G	NP_055178.3:p.Asp2600Glu
XM_005266338.1:c.7827T>G	XP_005266395.1:p.Asp2609Glu
XM_011535038.1:c.7851T>G	XP_011533340.1:p.Asp2617Glu
XM_011535039.1:c.7818T>G	XP_011533341.1:p.Asp2606Glu
XM_005266338.2:c.7827T>G	XP_005266395.1:p.Asp2609Glu
XM_011535039.2:c.7818T>G	XP_011533341.1:p.Asp2606Glu
XM_017020539.1:c.7791T>G	XP_016876028.1:p.Asp2597Glu
XM_024449337.1:c.7827T>G	XP_024305105.1:p.Asp2609Glu
NM_014363.6:c.7800T>G MANE Select	NP_055178.3:p.Asp2600Glu
NM_001278055.2:c.7359T>G	NP_001264984.1:p.Asp2453Glu