Canonical Allele Identifier: CA2078645166

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341777_23341783delinsGTTCTTT , CM000675.2:g.23341777_23341783delinsGTTCTTT	GRCh38
NC_000013.10:g.23915916_23915922delinsGTTCTTT , CM000675.1:g.23915916_23915922delinsGTTCTTT	GRCh37
NC_000013.9:g.22813916_22813922delinsGTTCTTT	NCBI36
NG_012342.1:g.96920_96926delinsAAAGAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12002_2185+12008delinsAAAGAAC	ENSP00000508399.1:n.2185+12002_2185+12008delinsAAAGAAC
ENST00000682944.1:c.2213-93_2213-87delinsAAAGAAC	ENSP00000507173.1:n.2213-93_2213-87delinsAAAGAAC
ENST00000683210.1:c.2185+12002_2185+12008delinsAAAGAAC	ENSP00000506739.1:n.2185+12002_2185+12008delinsAAAGAAC
ENST00000683270.1:c.2177-93_2177-87delinsAAAGAAC	ENSP00000507624.1:n.2177-93_2177-87delinsAAAGAAC
ENST00000683367.1:c.2176+12002_2176+12008delinsAAAGAAC	ENSP00000507780.1:n.2176+12002_2176+12008delinsAAAGAAC
ENST00000683489.1:c.2186-93_2186-87delinsAAAGAAC	ENSP00000508403.1:n.2186-93_2186-87delinsAAAGAAC
ENST00000683680.1:c.2213-93_2213-87delinsAAAGAAC	ENSP00000507223.1:n.2213-93_2213-87delinsAAAGAAC
ENST00000684163.1:c.2203+5028_2203+5034delinsAAAGAAC	ENSP00000508262.1:n.2203+5028_2203+5034delinsAAAGAAC
ENST00000684196.1:n.4542+12002_4542+12008delinsAAAGAAC
ENST00000684325.1:c.2185+12002_2185+12008delinsAAAGAAC	ENSP00000508121.1:n.2185+12002_2185+12008delinsAAAGAAC
ENST00000684385.1:c.2220+5028_2220+5034delinsAAAGAAC	ENSP00000507855.1:n.2220+5028_2220+5034delinsAAAGAAC
ENST00000684497.1:c.2185+12002_2185+12008delinsAAAGAAC	ENSP00000507057.1:n.2185+12002_2185+12008delinsAAAGAAC
ENST00000382292.9:c.2186-93_2186-87delinsAAAGAAC MANE Select	ENSP00000371729.3:n.2186-93_2186-87delinsAAAGAAC
ENST00000423156.2:c.2185+12002_2185+12008delinsAAAGAAC	ENSP00000390925.2:n.2185+12002_2185+12008delinsAAAGAAC
ENST00000455470.6:c.2186-93_2186-87delinsAAAGAAC	ENSP00000406565.2:n.2186-93_2186-87delinsAAAGAAC
ENST00000382292.7:c.2186-93_2186-87delinsAAAGAAC	ENSP00000371729.3:n.2186-93_2186-87delinsAAAGAAC
ENST00000382298.7:c.2186-93_2186-87delinsAAAGAAC	ENSP00000371735.3:n.2186-93_2186-87delinsAAAGAAC
ENST00000402364.1:c.-65-93_-65-87delinsAAAGAAC	ENSP00000385844.1:n.-65-93_-65-87delinsAAAGAAC
ENST00000423156.1:c.1057+12002_1057+12008delinsAAAGAAC	ENSP00000390925.1:n.1057+12002_1057+12008delinsAAAGAAC
ENST00000455470.5:c.1884-93_1884-87delinsAAAGAAC
NM_001278055.1:c.1745-93_1745-87delinsAAAGAAC	NP_001264984.1:n.1745-93_1745-87delinsAAAGAAC
NM_014363.5:c.2186-93_2186-87delinsAAAGAAC	NP_055178.3:n.2186-93_2186-87delinsAAAGAAC
XM_005266338.1:c.2213-93_2213-87delinsAAAGAAC	XP_005266395.1:n.2213-93_2213-87delinsAAAGAAC
XM_011535038.1:c.2237-93_2237-87delinsAAAGAAC	XP_011533340.1:n.2237-93_2237-87delinsAAAGAAC
XM_011535039.1:c.2204-93_2204-87delinsAAAGAAC	XP_011533341.1:n.2204-93_2204-87delinsAAAGAAC
XM_005266338.2:c.2213-93_2213-87delinsAAAGAAC	XP_005266395.1:n.2213-93_2213-87delinsAAAGAAC
XM_011535039.2:c.2204-93_2204-87delinsAAAGAAC	XP_011533341.1:n.2204-93_2204-87delinsAAAGAAC
XM_017020539.1:c.2177-93_2177-87delinsAAAGAAC	XP_016876028.1:n.2177-93_2177-87delinsAAAGAAC
XM_024449337.1:c.2213-93_2213-87delinsAAAGAAC	XP_024305105.1:n.2213-93_2213-87delinsAAAGAAC
NM_014363.6:c.2186-93_2186-87delinsAAAGAAC MANE Select	NP_055178.3:n.2186-93_2186-87delinsAAAGAAC
NM_001278055.2:c.1745-93_1745-87delinsAAAGAAC	NP_001264984.1:n.1745-93_1745-87delinsAAAGAAC