Canonical Allele Identifier: CA483160760

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23910473A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336334A>G , CM000675.2:g.23336334A>G	GRCh38
NC_000013.10:g.23910473A>G , CM000675.1:g.23910473A>G	GRCh37
NC_000013.9:g.22808473A>G	NCBI36
NG_012342.1:g.102369T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17451T>C	ENSP00000508399.1:n.2185+17451T>C
ENST00000682944.1:c.7569T>C	ENSP00000507173.1:p.Cys2523=
ENST00000683210.1:c.2185+17451T>C	ENSP00000506739.1:n.2185+17451T>C
ENST00000683270.1:c.6445+1088T>C	ENSP00000507624.1:n.6445+1088T>C
ENST00000683367.1:c.2177-6850T>C	ENSP00000507780.1:n.2177-6850T>C
ENST00000683489.1:c.2291+5251T>C	ENSP00000508403.1:n.2291+5251T>C
ENST00000683680.1:c.2318+5251T>C	ENSP00000507223.1:n.2318+5251T>C
ENST00000684163.1:c.2204-6850T>C	ENSP00000508262.1:n.2204-6850T>C
ENST00000684196.1:n.4543-6850T>C
ENST00000684325.1:c.2186-14660T>C	ENSP00000508121.1:n.2186-14660T>C
ENST00000684385.1:c.2221-6850T>C	ENSP00000507855.1:n.2221-6850T>C
ENST00000684497.1:c.2186-13690T>C	ENSP00000507057.1:n.2186-13690T>C
ENST00000382292.9:c.7542T>C MANE Select	ENSP00000371729.3:p.Cys2514=
ENST00000423156.2:c.2186-6850T>C	ENSP00000390925.2:n.2186-6850T>C
ENST00000455470.6:c.2431+5111T>C	ENSP00000406565.2:n.2431+5111T>C
ENST00000382292.7:c.7542T>C	ENSP00000371729.3:p.Cys2514=
ENST00000382298.7:c.7542T>C	ENSP00000371735.3:p.Cys2514=
ENST00000402364.1:c.5292T>C	ENSP00000385844.1:p.Cys1764=
ENST00000423156.1:c.1058-6850T>C	ENSP00000390925.1:n.1058-6850T>C
ENST00000455470.5:c.2129+5111T>C
NM_001278055.1:c.7101T>C	NP_001264984.1:p.Cys2367=
NM_014363.5:c.7542T>C	NP_055178.3:p.Cys2514=
XM_005266338.1:c.7569T>C	XP_005266395.1:p.Cys2523=
XM_011535038.1:c.7593T>C	XP_011533340.1:p.Cys2531=
XM_011535039.1:c.7560T>C	XP_011533341.1:p.Cys2520=
XM_005266338.2:c.7569T>C	XP_005266395.1:p.Cys2523=
XM_011535039.2:c.7560T>C	XP_011533341.1:p.Cys2520=
XM_017020539.1:c.7533T>C	XP_016876028.1:p.Cys2511=
XM_024449337.1:c.7569T>C	XP_024305105.1:p.Cys2523=
NM_014363.6:c.7542T>C MANE Select	NP_055178.3:p.Cys2514=
NM_001278055.2:c.7101T>C	NP_001264984.1:p.Cys2367=