Canonical Allele Identifier: CA483162166

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23912645A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23338506A>G , CM000675.2:g.23338506A>G	GRCh38
NC_000013.10:g.23912645A>G , CM000675.1:g.23912645A>G	GRCh37
NC_000013.9:g.22810645A>G	NCBI36
NG_012342.1:g.100197T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+15279T>C	ENSP00000508399.1:n.2185+15279T>C
ENST00000682944.1:c.5397T>C	ENSP00000507173.1:p.Ala1799=
ENST00000683210.1:c.2185+15279T>C	ENSP00000506739.1:n.2185+15279T>C
ENST00000683270.1:c.5361T>C	ENSP00000507624.1:p.Ala1787=
ENST00000683367.1:c.2177-9022T>C	ENSP00000507780.1:n.2177-9022T>C
ENST00000683489.1:c.2291+3079T>C	ENSP00000508403.1:n.2291+3079T>C
ENST00000683680.1:c.2318+3079T>C	ENSP00000507223.1:n.2318+3079T>C
ENST00000684163.1:c.2203+8305T>C	ENSP00000508262.1:n.2203+8305T>C
ENST00000684196.1:n.4543-9022T>C
ENST00000684325.1:c.2185+15279T>C	ENSP00000508121.1:n.2185+15279T>C
ENST00000684385.1:c.2220+8305T>C	ENSP00000507855.1:n.2220+8305T>C
ENST00000684497.1:c.2185+15279T>C	ENSP00000507057.1:n.2185+15279T>C
ENST00000382292.9:c.5370T>C MANE Select	ENSP00000371729.3:p.Ala1790=
ENST00000423156.2:c.2186-9022T>C	ENSP00000390925.2:n.2186-9022T>C
ENST00000455470.6:c.2431+2939T>C	ENSP00000406565.2:n.2431+2939T>C
ENST00000382292.7:c.5370T>C	ENSP00000371729.3:p.Ala1790=
ENST00000382298.7:c.5370T>C	ENSP00000371735.3:p.Ala1790=
ENST00000402364.1:c.3120T>C	ENSP00000385844.1:p.Ala1040=
ENST00000423156.1:c.1058-9022T>C	ENSP00000390925.1:n.1058-9022T>C
ENST00000455470.5:c.2129+2939T>C
NM_001278055.1:c.4929T>C	NP_001264984.1:p.Ala1643=
NM_014363.5:c.5370T>C	NP_055178.3:p.Ala1790=
XM_005266338.1:c.5397T>C	XP_005266395.1:p.Ala1799=
XM_011535038.1:c.5421T>C	XP_011533340.1:p.Ala1807=
XM_011535039.1:c.5388T>C	XP_011533341.1:p.Ala1796=
XM_005266338.2:c.5397T>C	XP_005266395.1:p.Ala1799=
XM_011535039.2:c.5388T>C	XP_011533341.1:p.Ala1796=
XM_017020539.1:c.5361T>C	XP_016876028.1:p.Ala1787=
XM_024449337.1:c.5397T>C	XP_024305105.1:p.Ala1799=
NM_014363.6:c.5370T>C MANE Select	NP_055178.3:p.Ala1790=
NM_001278055.2:c.4929T>C	NP_001264984.1:p.Ala1643=