Canonical Allele Identifier: CA2078645355
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23341806_23341808delinsTGA , CM000675.2:g.23341806_23341808delinsTGA GRCh38
NC_000013.10:g.23915945_23915947delinsTGA , CM000675.1:g.23915945_23915947delinsTGA GRCh37
NC_000013.9:g.22813945_22813947delinsTGA NCBI36
NG_012342.1:g.96895_96897delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+11977_2185+11979delinsTCA ENSP00000508399.1:n.2185+11977_2185+11979delinsTCA
ENST00000682944.1:c.2213-118_2213-116delinsTCA ENSP00000507173.1:n.2213-118_2213-116delinsTCA
ENST00000683210.1:c.2185+11977_2185+11979delinsTCA ENSP00000506739.1:n.2185+11977_2185+11979delinsTCA
ENST00000683270.1:c.2177-118_2177-116delinsTCA ENSP00000507624.1:n.2177-118_2177-116delinsTCA
ENST00000683367.1:c.2176+11977_2176+11979delinsTCA ENSP00000507780.1:n.2176+11977_2176+11979delinsTCA
ENST00000683489.1:c.2186-118_2186-116delinsTCA ENSP00000508403.1:n.2186-118_2186-116delinsTCA
ENST00000683680.1:c.2213-118_2213-116delinsTCA ENSP00000507223.1:n.2213-118_2213-116delinsTCA
ENST00000684163.1:c.2203+5003_2203+5005delinsTCA ENSP00000508262.1:n.2203+5003_2203+5005delinsTCA
ENST00000684196.1:n.4542+11977_4542+11979delinsTCA
ENST00000684325.1:c.2185+11977_2185+11979delinsTCA ENSP00000508121.1:n.2185+11977_2185+11979delinsTCA
ENST00000684385.1:c.2220+5003_2220+5005delinsTCA ENSP00000507855.1:n.2220+5003_2220+5005delinsTCA
ENST00000684497.1:c.2185+11977_2185+11979delinsTCA ENSP00000507057.1:n.2185+11977_2185+11979delinsTCA
ENST00000382292.9:c.2186-118_2186-116delinsTCA MANE Select ENSP00000371729.3:n.2186-118_2186-116delinsTCA
ENST00000423156.2:c.2185+11977_2185+11979delinsTCA ENSP00000390925.2:n.2185+11977_2185+11979delinsTCA
ENST00000455470.6:c.2186-118_2186-116delinsTCA ENSP00000406565.2:n.2186-118_2186-116delinsTCA
ENST00000382292.7:c.2186-118_2186-116delinsTCA ENSP00000371729.3:n.2186-118_2186-116delinsTCA
ENST00000382298.7:c.2186-118_2186-116delinsTCA ENSP00000371735.3:n.2186-118_2186-116delinsTCA
ENST00000402364.1:c.-65-118_-65-116delinsTCA ENSP00000385844.1:n.-65-118_-65-116delinsTCA
ENST00000423156.1:c.1057+11977_1057+11979delinsTCA ENSP00000390925.1:n.1057+11977_1057+11979delinsTCA
ENST00000455470.5:c.1884-118_1884-116delinsTCA
NM_001278055.1:c.1745-118_1745-116delinsTCA NP_001264984.1:n.1745-118_1745-116delinsTCA
NM_014363.5:c.2186-118_2186-116delinsTCA NP_055178.3:n.2186-118_2186-116delinsTCA
XM_005266338.1:c.2213-118_2213-116delinsTCA XP_005266395.1:n.2213-118_2213-116delinsTCA
XM_011535038.1:c.2237-118_2237-116delinsTCA XP_011533340.1:n.2237-118_2237-116delinsTCA
XM_011535039.1:c.2204-118_2204-116delinsTCA XP_011533341.1:n.2204-118_2204-116delinsTCA
XM_005266338.2:c.2213-118_2213-116delinsTCA XP_005266395.1:n.2213-118_2213-116delinsTCA
XM_011535039.2:c.2204-118_2204-116delinsTCA XP_011533341.1:n.2204-118_2204-116delinsTCA
XM_017020539.1:c.2177-118_2177-116delinsTCA XP_016876028.1:n.2177-118_2177-116delinsTCA
XM_024449337.1:c.2213-118_2213-116delinsTCA XP_024305105.1:n.2213-118_2213-116delinsTCA
NM_014363.6:c.2186-118_2186-116delinsTCA MANE Select NP_055178.3:n.2186-118_2186-116delinsTCA
NM_001278055.2:c.1745-118_1745-116delinsTCA NP_001264984.1:n.1745-118_1745-116delinsTCA