Canonical Allele Identifier: CA608625966
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs1491485499

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23341779_23341780insA , CM000675.2:g.23341779_23341780insA GRCh38
NC_000013.10:g.23915918_23915919insA , CM000675.1:g.23915918_23915919insA GRCh37
NC_000013.9:g.22813918_22813919insA NCBI36
NG_012342.1:g.96923_96924insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+12005_2185+12006insT ENSP00000508399.1:n.2185+12005_2185+12006insT
ENST00000682944.1:c.2213-90_2213-89insT ENSP00000507173.1:n.2213-90_2213-89insT
ENST00000683210.1:c.2185+12005_2185+12006insT ENSP00000506739.1:n.2185+12005_2185+12006insT
ENST00000683270.1:c.2177-90_2177-89insT ENSP00000507624.1:n.2177-90_2177-89insT
ENST00000683367.1:c.2176+12005_2176+12006insT ENSP00000507780.1:n.2176+12005_2176+12006insT
ENST00000683489.1:c.2186-90_2186-89insT ENSP00000508403.1:n.2186-90_2186-89insT
ENST00000683680.1:c.2213-90_2213-89insT ENSP00000507223.1:n.2213-90_2213-89insT
ENST00000684163.1:c.2203+5031_2203+5032insT ENSP00000508262.1:n.2203+5031_2203+5032insT
ENST00000684196.1:n.4542+12005_4542+12006insT
ENST00000684325.1:c.2185+12005_2185+12006insT ENSP00000508121.1:n.2185+12005_2185+12006insT
ENST00000684385.1:c.2220+5031_2220+5032insT ENSP00000507855.1:n.2220+5031_2220+5032insT
ENST00000684497.1:c.2185+12005_2185+12006insT ENSP00000507057.1:n.2185+12005_2185+12006insT
ENST00000382292.9:c.2186-90_2186-89insT MANE Select ENSP00000371729.3:n.2186-90_2186-89insT
ENST00000423156.2:c.2185+12005_2185+12006insT ENSP00000390925.2:n.2185+12005_2185+12006insT
ENST00000455470.6:c.2186-90_2186-89insT ENSP00000406565.2:n.2186-90_2186-89insT
ENST00000382292.7:c.2186-90_2186-89insT ENSP00000371729.3:n.2186-90_2186-89insT
ENST00000382298.7:c.2186-90_2186-89insT ENSP00000371735.3:n.2186-90_2186-89insT
ENST00000402364.1:c.-65-90_-65-89insT ENSP00000385844.1:n.-65-90_-65-89insT
ENST00000423156.1:c.1057+12005_1057+12006insT ENSP00000390925.1:n.1057+12005_1057+12006insT
ENST00000455470.5:c.1884-90_1884-89insT
NM_001278055.1:c.1745-90_1745-89insT NP_001264984.1:n.1745-90_1745-89insT
NM_014363.5:c.2186-90_2186-89insT NP_055178.3:n.2186-90_2186-89insT
XM_005266338.1:c.2213-90_2213-89insT XP_005266395.1:n.2213-90_2213-89insT
XM_011535038.1:c.2237-90_2237-89insT XP_011533340.1:n.2237-90_2237-89insT
XM_011535039.1:c.2204-90_2204-89insT XP_011533341.1:n.2204-90_2204-89insT
XM_005266338.2:c.2213-90_2213-89insT XP_005266395.1:n.2213-90_2213-89insT
XM_011535039.2:c.2204-90_2204-89insT XP_011533341.1:n.2204-90_2204-89insT
XM_017020539.1:c.2177-90_2177-89insT XP_016876028.1:n.2177-90_2177-89insT
XM_024449337.1:c.2213-90_2213-89insT XP_024305105.1:n.2213-90_2213-89insT
NM_014363.6:c.2186-90_2186-89insT MANE Select NP_055178.3:n.2186-90_2186-89insT
NM_001278055.2:c.1745-90_1745-89insT NP_001264984.1:n.1745-90_1745-89insT