Canonical Allele Identifier: CA387520505

Gene: SACS

Linked Data

• ClinVar Variation Id: 2150983
• ClinVar RCV Id: RCV003072015
• gnomAD v4: 13-23336979-T-G
• MyVariant Identifiers: chr13:g.23911118T>G (hg19) ; chr13:g.23336979T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336979T>G , CM000675.2:g.23336979T>G	GRCh38
NC_000013.10:g.23911118T>G , CM000675.1:g.23911118T>G	GRCh37
NC_000013.9:g.22809118T>G	NCBI36
NG_012342.1:g.101724A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16806A>C	ENSP00000508399.1:n.2185+16806A>C
ENST00000682944.1:c.6924A>C	ENSP00000507173.1:p.Glu2308Asp
ENST00000683210.1:c.2185+16806A>C	ENSP00000506739.1:n.2185+16806A>C
ENST00000683270.1:c.6445+443A>C	ENSP00000507624.1:n.6445+443A>C
ENST00000683367.1:c.2177-7495A>C	ENSP00000507780.1:n.2177-7495A>C
ENST00000683489.1:c.2291+4606A>C	ENSP00000508403.1:n.2291+4606A>C
ENST00000683680.1:c.2318+4606A>C	ENSP00000507223.1:n.2318+4606A>C
ENST00000684163.1:c.2204-7495A>C	ENSP00000508262.1:n.2204-7495A>C
ENST00000684196.1:n.4543-7495A>C
ENST00000684325.1:c.2186-15305A>C	ENSP00000508121.1:n.2186-15305A>C
ENST00000684385.1:c.2221-7495A>C	ENSP00000507855.1:n.2221-7495A>C
ENST00000684497.1:c.2186-14335A>C	ENSP00000507057.1:n.2186-14335A>C
ENST00000382292.9:c.6897A>C MANE Select	ENSP00000371729.3:p.Glu2299Asp
ENST00000423156.2:c.2186-7495A>C	ENSP00000390925.2:n.2186-7495A>C
ENST00000455470.6:c.2431+4466A>C	ENSP00000406565.2:n.2431+4466A>C
ENST00000382292.7:c.6897A>C	ENSP00000371729.3:p.Glu2299Asp
ENST00000382298.7:c.6897A>C	ENSP00000371735.3:p.Glu2299Asp
ENST00000402364.1:c.4647A>C	ENSP00000385844.1:p.Glu1549Asp
ENST00000423156.1:c.1058-7495A>C	ENSP00000390925.1:n.1058-7495A>C
ENST00000455470.5:c.2129+4466A>C
NM_001278055.1:c.6456A>C	NP_001264984.1:p.Glu2152Asp
NM_014363.5:c.6897A>C	NP_055178.3:p.Glu2299Asp
XM_005266338.1:c.6924A>C	XP_005266395.1:p.Glu2308Asp
XM_011535038.1:c.6948A>C	XP_011533340.1:p.Glu2316Asp
XM_011535039.1:c.6915A>C	XP_011533341.1:p.Glu2305Asp
XM_005266338.2:c.6924A>C	XP_005266395.1:p.Glu2308Asp
XM_011535039.2:c.6915A>C	XP_011533341.1:p.Glu2305Asp
XM_017020539.1:c.6888A>C	XP_016876028.1:p.Glu2296Asp
XM_024449337.1:c.6924A>C	XP_024305105.1:p.Glu2308Asp
NM_014363.6:c.6897A>C MANE Select	NP_055178.3:p.Glu2299Asp
NM_001278055.2:c.6456A>C	NP_001264984.1:p.Glu2152Asp