Canonical Allele Identifier: CA387506565
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330975T>G , CM000675.2:g.23330975T>G GRCh38
NC_000013.10:g.23905114T>G , CM000675.1:g.23905114T>G GRCh37
NC_000013.9:g.22803114T>G NCBI36
NG_012342.1:g.107728A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2186-18860A>C ENSP00000508399.1:n.2186-18860A>C
ENST00000682944.1:c.12928A>C ENSP00000507173.1:p.Asn4310His
ENST00000683210.1:c.2185+22810A>C ENSP00000506739.1:n.2185+22810A>C
ENST00000683270.1:c.6446-1491A>C ENSP00000507624.1:n.6446-1491A>C
ENST00000683367.1:c.2177-1491A>C ENSP00000507780.1:n.2177-1491A>C
ENST00000683489.1:c.2292-1023A>C ENSP00000508403.1:n.2292-1023A>C
ENST00000683680.1:c.2319-1023A>C ENSP00000507223.1:n.2319-1023A>C
ENST00000684163.1:c.2204-1491A>C ENSP00000508262.1:n.2204-1491A>C
ENST00000684196.1:n.4543-1491A>C
ENST00000684325.1:c.2186-9301A>C ENSP00000508121.1:n.2186-9301A>C
ENST00000684385.1:c.2221-1491A>C ENSP00000507855.1:n.2221-1491A>C
ENST00000684497.1:c.2186-8331A>C ENSP00000507057.1:n.2186-8331A>C
ENST00000382292.9:c.12901A>C MANE Select ENSP00000371729.3:p.Asn4301His
ENST00000423156.2:c.2186-1491A>C ENSP00000390925.2:n.2186-1491A>C
ENST00000455470.6:c.2432-1491A>C ENSP00000406565.2:n.2432-1491A>C
ENST00000382292.7:c.12901A>C ENSP00000371729.3:p.Asn4301His
ENST00000382298.7:c.12901A>C ENSP00000371735.3:p.Asn4301His
ENST00000402364.1:c.10651A>C ENSP00000385844.1:p.Asn3551His
ENST00000423156.1:c.1058-1491A>C ENSP00000390925.1:n.1058-1491A>C
ENST00000455470.5:c.2130-1491A>C
NM_001278055.1:c.12460A>C NP_001264984.1:p.Asn4154His
NM_014363.5:c.12901A>C NP_055178.3:p.Asn4301His
XM_005266338.1:c.12928A>C XP_005266395.1:p.Asn4310His
XM_011535038.1:c.12952A>C XP_011533340.1:p.Asn4318His
XM_011535039.1:c.12919A>C XP_011533341.1:p.Asn4307His
XM_005266338.2:c.12928A>C XP_005266395.1:p.Asn4310His
XM_011535039.2:c.12919A>C XP_011533341.1:p.Asn4307His
XM_017020539.1:c.12892A>C XP_016876028.1:p.Asn4298His
XM_024449337.1:c.12928A>C XP_024305105.1:p.Asn4310His
NM_014363.6:c.12901A>C MANE Select NP_055178.3:p.Asn4301His
NM_001278055.2:c.12460A>C NP_001264984.1:p.Asn4154His