Canonical Allele Identifier: CA483162402
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23913260T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339121T>G , CM000675.2:g.23339121T>G GRCh38
NC_000013.10:g.23913260T>G , CM000675.1:g.23913260T>G GRCh37
NC_000013.9:g.22811260T>G NCBI36
NG_012342.1:g.99582A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+14664A>C ENSP00000508399.1:n.2185+14664A>C
ENST00000682944.1:c.4782A>C ENSP00000507173.1:p.Ile1594=
ENST00000683210.1:c.2185+14664A>C ENSP00000506739.1:n.2185+14664A>C
ENST00000683270.1:c.4746A>C ENSP00000507624.1:p.Ile1582=
ENST00000683367.1:c.2177-9637A>C ENSP00000507780.1:n.2177-9637A>C
ENST00000683489.1:c.2291+2464A>C ENSP00000508403.1:n.2291+2464A>C
ENST00000683680.1:c.2318+2464A>C ENSP00000507223.1:n.2318+2464A>C
ENST00000684163.1:c.2203+7690A>C ENSP00000508262.1:n.2203+7690A>C
ENST00000684196.1:n.4543-9637A>C
ENST00000684325.1:c.2185+14664A>C ENSP00000508121.1:n.2185+14664A>C
ENST00000684385.1:c.2220+7690A>C ENSP00000507855.1:n.2220+7690A>C
ENST00000684497.1:c.2185+14664A>C ENSP00000507057.1:n.2185+14664A>C
ENST00000382292.9:c.4755A>C MANE Select ENSP00000371729.3:p.Ile1585=
ENST00000423156.2:c.2186-9637A>C ENSP00000390925.2:n.2186-9637A>C
ENST00000455470.6:c.2431+2324A>C ENSP00000406565.2:n.2431+2324A>C
ENST00000382292.7:c.4755A>C ENSP00000371729.3:p.Ile1585=
ENST00000382298.7:c.4755A>C ENSP00000371735.3:p.Ile1585=
ENST00000402364.1:c.2505A>C ENSP00000385844.1:p.Ile835=
ENST00000423156.1:c.1058-9637A>C ENSP00000390925.1:n.1058-9637A>C
ENST00000455470.5:c.2129+2324A>C
NM_001278055.1:c.4314A>C NP_001264984.1:p.Ile1438=
NM_014363.5:c.4755A>C NP_055178.3:p.Ile1585=
XM_005266338.1:c.4782A>C XP_005266395.1:p.Ile1594=
XM_011535038.1:c.4806A>C XP_011533340.1:p.Ile1602=
XM_011535039.1:c.4773A>C XP_011533341.1:p.Ile1591=
XM_005266338.2:c.4782A>C XP_005266395.1:p.Ile1594=
XM_011535039.2:c.4773A>C XP_011533341.1:p.Ile1591=
XM_017020539.1:c.4746A>C XP_016876028.1:p.Ile1582=
XM_024449337.1:c.4782A>C XP_024305105.1:p.Ile1594=
NM_014363.6:c.4755A>C MANE Select NP_055178.3:p.Ile1585=
NM_001278055.2:c.4314A>C NP_001264984.1:p.Ile1438=