Canonical Allele Identifier: CA483160620

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909900T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23335761T>G , CM000675.2:g.23335761T>G	GRCh38
NC_000013.10:g.23909900T>G , CM000675.1:g.23909900T>G	GRCh37
NC_000013.9:g.22807900T>G	NCBI36
NG_012342.1:g.102942A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18024A>C	ENSP00000508399.1:n.2185+18024A>C
ENST00000682944.1:c.8142A>C	ENSP00000507173.1:p.Ala2714=
ENST00000683210.1:c.2185+18024A>C	ENSP00000506739.1:n.2185+18024A>C
ENST00000683270.1:c.6445+1661A>C	ENSP00000507624.1:n.6445+1661A>C
ENST00000683367.1:c.2177-6277A>C	ENSP00000507780.1:n.2177-6277A>C
ENST00000683489.1:c.2292-5809A>C	ENSP00000508403.1:n.2292-5809A>C
ENST00000683680.1:c.2319-5809A>C	ENSP00000507223.1:n.2319-5809A>C
ENST00000684163.1:c.2204-6277A>C	ENSP00000508262.1:n.2204-6277A>C
ENST00000684196.1:n.4543-6277A>C
ENST00000684325.1:c.2186-14087A>C	ENSP00000508121.1:n.2186-14087A>C
ENST00000684385.1:c.2221-6277A>C	ENSP00000507855.1:n.2221-6277A>C
ENST00000684497.1:c.2186-13117A>C	ENSP00000507057.1:n.2186-13117A>C
ENST00000382292.9:c.8115A>C MANE Select	ENSP00000371729.3:p.Ala2705=
ENST00000423156.2:c.2186-6277A>C	ENSP00000390925.2:n.2186-6277A>C
ENST00000455470.6:c.2431+5684A>C	ENSP00000406565.2:n.2431+5684A>C
ENST00000382292.7:c.8115A>C	ENSP00000371729.3:p.Ala2705=
ENST00000382298.7:c.8115A>C	ENSP00000371735.3:p.Ala2705=
ENST00000402364.1:c.5865A>C	ENSP00000385844.1:p.Ala1955=
ENST00000423156.1:c.1058-6277A>C	ENSP00000390925.1:n.1058-6277A>C
ENST00000455470.5:c.2129+5684A>C
NM_001278055.1:c.7674A>C	NP_001264984.1:p.Ala2558=
NM_014363.5:c.8115A>C	NP_055178.3:p.Ala2705=
XM_005266338.1:c.8142A>C	XP_005266395.1:p.Ala2714=
XM_011535038.1:c.8166A>C	XP_011533340.1:p.Ala2722=
XM_011535039.1:c.8133A>C	XP_011533341.1:p.Ala2711=
XM_005266338.2:c.8142A>C	XP_005266395.1:p.Ala2714=
XM_011535039.2:c.8133A>C	XP_011533341.1:p.Ala2711=
XM_017020539.1:c.8106A>C	XP_016876028.1:p.Ala2702=
XM_024449337.1:c.8142A>C	XP_024305105.1:p.Ala2714=
NM_014363.6:c.8115A>C MANE Select	NP_055178.3:p.Ala2705=
NM_001278055.2:c.7674A>C	NP_001264984.1:p.Ala2558=