Canonical Allele Identifier: CA387506169
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330849C>G , CM000675.2:g.23330849C>G GRCh38
NC_000013.10:g.23904988C>G , CM000675.1:g.23904988C>G GRCh37
NC_000013.9:g.22802988C>G NCBI36
NG_012342.1:g.107854G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2186-18734G>C ENSP00000508399.1:n.2186-18734G>C
ENST00000682944.1:c.13054G>C ENSP00000507173.1:p.Glu4352Gln
ENST00000683210.1:c.2185+22936G>C ENSP00000506739.1:n.2185+22936G>C
ENST00000683270.1:c.6446-1365G>C ENSP00000507624.1:n.6446-1365G>C
ENST00000683367.1:c.2177-1365G>C ENSP00000507780.1:n.2177-1365G>C
ENST00000683489.1:c.2292-897G>C ENSP00000508403.1:n.2292-897G>C
ENST00000683680.1:c.2319-897G>C ENSP00000507223.1:n.2319-897G>C
ENST00000684163.1:c.2204-1365G>C ENSP00000508262.1:n.2204-1365G>C
ENST00000684196.1:n.4543-1365G>C
ENST00000684325.1:c.2186-9175G>C ENSP00000508121.1:n.2186-9175G>C
ENST00000684385.1:c.2221-1365G>C ENSP00000507855.1:n.2221-1365G>C
ENST00000684497.1:c.2186-8205G>C ENSP00000507057.1:n.2186-8205G>C
ENST00000382292.9:c.13027G>C MANE Select ENSP00000371729.3:p.Glu4343Gln
ENST00000423156.2:c.2186-1365G>C ENSP00000390925.2:n.2186-1365G>C
ENST00000455470.6:c.2432-1365G>C ENSP00000406565.2:n.2432-1365G>C
ENST00000382292.7:c.13027G>C ENSP00000371729.3:p.Glu4343Gln
ENST00000382298.7:c.13027G>C ENSP00000371735.3:p.Glu4343Gln
ENST00000402364.1:c.10777G>C ENSP00000385844.1:p.Glu3593Gln
ENST00000423156.1:c.1058-1365G>C ENSP00000390925.1:n.1058-1365G>C
ENST00000455470.5:c.2130-1365G>C
NM_001278055.1:c.12586G>C NP_001264984.1:p.Glu4196Gln
NM_014363.5:c.13027G>C NP_055178.3:p.Glu4343Gln
XM_005266338.1:c.13054G>C XP_005266395.1:p.Glu4352Gln
XM_011535038.1:c.13078G>C XP_011533340.1:p.Glu4360Gln
XM_011535039.1:c.13045G>C XP_011533341.1:p.Glu4349Gln
XM_005266338.2:c.13054G>C XP_005266395.1:p.Glu4352Gln
XM_011535039.2:c.13045G>C XP_011533341.1:p.Glu4349Gln
XM_017020539.1:c.13018G>C XP_016876028.1:p.Glu4340Gln
XM_024449337.1:c.13054G>C XP_024305105.1:p.Glu4352Gln
NM_014363.6:c.13027G>C MANE Select NP_055178.3:p.Glu4343Gln
NM_001278055.2:c.12586G>C NP_001264984.1:p.Glu4196Gln