Canonical Allele Identifier: CA2078623813
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23335618T= , CM000675.2:g.23335618T= GRCh38
NC_000013.10:g.23909757T= , CM000675.1:g.23909757T= GRCh37
NC_000013.9:g.22807757T= NCBI36
NG_012342.1:g.103085A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18167A= ENSP00000508399.1:n.2185+18167A=
ENST00000682944.1:c.8285A= ENSP00000507173.1:p.Asp2762=
ENST00000683210.1:c.2185+18167A= ENSP00000506739.1:n.2185+18167A=
ENST00000683270.1:c.6445+1804A= ENSP00000507624.1:n.6445+1804A=
ENST00000683367.1:c.2177-6134A= ENSP00000507780.1:n.2177-6134A=
ENST00000683489.1:c.2292-5666A= ENSP00000508403.1:n.2292-5666A=
ENST00000683680.1:c.2319-5666A= ENSP00000507223.1:n.2319-5666A=
ENST00000684163.1:c.2204-6134A= ENSP00000508262.1:n.2204-6134A=
ENST00000684196.1:n.4543-6134A=
ENST00000684325.1:c.2186-13944A= ENSP00000508121.1:n.2186-13944A=
ENST00000684385.1:c.2221-6134A= ENSP00000507855.1:n.2221-6134A=
ENST00000684497.1:c.2186-12974A= ENSP00000507057.1:n.2186-12974A=
ENST00000382292.9:c.8258A= MANE Select ENSP00000371729.3:p.Asp2753=
ENST00000423156.2:c.2186-6134A= ENSP00000390925.2:n.2186-6134A=
ENST00000455470.6:c.2431+5827A= ENSP00000406565.2:n.2431+5827A=
ENST00000382292.7:c.8258A= ENSP00000371729.3:p.Asp2753=
ENST00000382298.7:c.8258A= ENSP00000371735.3:p.Asp2753=
ENST00000402364.1:c.6008A= ENSP00000385844.1:p.Asp2003=
ENST00000423156.1:c.1058-6134A= ENSP00000390925.1:n.1058-6134A=
ENST00000455470.5:c.2129+5827A=
NM_001278055.1:c.7817A= NP_001264984.1:p.Asp2606=
NM_014363.5:c.8258A= NP_055178.3:p.Asp2753=
XM_005266338.1:c.8285A= XP_005266395.1:p.Asp2762=
XM_011535038.1:c.8309A= XP_011533340.1:p.Asp2770=
XM_011535039.1:c.8276A= XP_011533341.1:p.Asp2759=
XM_005266338.2:c.8285A= XP_005266395.1:p.Asp2762=
XM_011535039.2:c.8276A= XP_011533341.1:p.Asp2759=
XM_017020539.1:c.8249A= XP_016876028.1:p.Asp2750=
XM_024449337.1:c.8285A= XP_024305105.1:p.Asp2762=
NM_014363.6:c.8258A= MANE Select NP_055178.3:p.Asp2753=
NM_001278055.2:c.7817A= NP_001264984.1:p.Asp2606=