Canonical Allele Identifier: CA2078623774
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23335599T= , CM000675.2:g.23335599T= GRCh38
NC_000013.10:g.23909738T= , CM000675.1:g.23909738T= GRCh37
NC_000013.9:g.22807738T= NCBI36
NG_012342.1:g.103104A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18186A= ENSP00000508399.1:n.2185+18186A=
ENST00000682944.1:c.8304A= ENSP00000507173.1:p.Leu2768=
ENST00000683210.1:c.2185+18186A= ENSP00000506739.1:n.2185+18186A=
ENST00000683270.1:c.6445+1823A= ENSP00000507624.1:n.6445+1823A=
ENST00000683367.1:c.2177-6115A= ENSP00000507780.1:n.2177-6115A=
ENST00000683489.1:c.2292-5647A= ENSP00000508403.1:n.2292-5647A=
ENST00000683680.1:c.2319-5647A= ENSP00000507223.1:n.2319-5647A=
ENST00000684163.1:c.2204-6115A= ENSP00000508262.1:n.2204-6115A=
ENST00000684196.1:n.4543-6115A=
ENST00000684325.1:c.2186-13925A= ENSP00000508121.1:n.2186-13925A=
ENST00000684385.1:c.2221-6115A= ENSP00000507855.1:n.2221-6115A=
ENST00000684497.1:c.2186-12955A= ENSP00000507057.1:n.2186-12955A=
ENST00000382292.9:c.8277A= MANE Select ENSP00000371729.3:p.Leu2759=
ENST00000423156.2:c.2186-6115A= ENSP00000390925.2:n.2186-6115A=
ENST00000455470.6:c.2431+5846A= ENSP00000406565.2:n.2431+5846A=
ENST00000382292.7:c.8277A= ENSP00000371729.3:p.Leu2759=
ENST00000382298.7:c.8277A= ENSP00000371735.3:p.Leu2759=
ENST00000402364.1:c.6027A= ENSP00000385844.1:p.Leu2009=
ENST00000423156.1:c.1058-6115A= ENSP00000390925.1:n.1058-6115A=
ENST00000455470.5:c.2129+5846A=
NM_001278055.1:c.7836A= NP_001264984.1:p.Leu2612=
NM_014363.5:c.8277A= NP_055178.3:p.Leu2759=
XM_005266338.1:c.8304A= XP_005266395.1:p.Leu2768=
XM_011535038.1:c.8328A= XP_011533340.1:p.Leu2776=
XM_011535039.1:c.8295A= XP_011533341.1:p.Leu2765=
XM_005266338.2:c.8304A= XP_005266395.1:p.Leu2768=
XM_011535039.2:c.8295A= XP_011533341.1:p.Leu2765=
XM_017020539.1:c.8268A= XP_016876028.1:p.Leu2756=
XM_024449337.1:c.8304A= XP_024305105.1:p.Leu2768=
NM_014363.6:c.8277A= MANE Select NP_055178.3:p.Leu2759=
NM_001278055.2:c.7836A= NP_001264984.1:p.Leu2612=