Canonical Allele Identifier: CA2622329194

Gene: SACS

Linked Data

• gnomAD v4: 13-23341798-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341799_23341800insCT , CM000675.2:g.23341799_23341800insCT	GRCh38
NC_000013.10:g.23915938_23915939insCT , CM000675.1:g.23915938_23915939insCT	GRCh37
NC_000013.9:g.22813938_22813939insCT	NCBI36
NG_012342.1:g.96904_96905insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+11986_2185+11987insGA	ENSP00000508399.1:n.2185+11986_2185+11987insGA
ENST00000682944.1:c.2213-109_2213-108insGA	ENSP00000507173.1:n.2213-109_2213-108insGA
ENST00000683210.1:c.2185+11986_2185+11987insGA	ENSP00000506739.1:n.2185+11986_2185+11987insGA
ENST00000683270.1:c.2177-109_2177-108insGA	ENSP00000507624.1:n.2177-109_2177-108insGA
ENST00000683367.1:c.2176+11986_2176+11987insGA	ENSP00000507780.1:n.2176+11986_2176+11987insGA
ENST00000683489.1:c.2186-109_2186-108insGA	ENSP00000508403.1:n.2186-109_2186-108insGA
ENST00000683680.1:c.2213-109_2213-108insGA	ENSP00000507223.1:n.2213-109_2213-108insGA
ENST00000684163.1:c.2203+5012_2203+5013insGA	ENSP00000508262.1:n.2203+5012_2203+5013insGA
ENST00000684196.1:n.4542+11986_4542+11987insGA
ENST00000684325.1:c.2185+11986_2185+11987insGA	ENSP00000508121.1:n.2185+11986_2185+11987insGA
ENST00000684385.1:c.2220+5012_2220+5013insGA	ENSP00000507855.1:n.2220+5012_2220+5013insGA
ENST00000684497.1:c.2185+11986_2185+11987insGA	ENSP00000507057.1:n.2185+11986_2185+11987insGA
ENST00000382292.9:c.2186-109_2186-108insGA MANE Select	ENSP00000371729.3:n.2186-109_2186-108insGA
ENST00000423156.2:c.2185+11986_2185+11987insGA	ENSP00000390925.2:n.2185+11986_2185+11987insGA
ENST00000455470.6:c.2186-109_2186-108insGA	ENSP00000406565.2:n.2186-109_2186-108insGA
ENST00000382292.7:c.2186-109_2186-108insGA	ENSP00000371729.3:n.2186-109_2186-108insGA
ENST00000382298.7:c.2186-109_2186-108insGA	ENSP00000371735.3:n.2186-109_2186-108insGA
ENST00000402364.1:c.-65-109_-65-108insGA	ENSP00000385844.1:n.-65-109_-65-108insGA
ENST00000423156.1:c.1057+11986_1057+11987insGA	ENSP00000390925.1:n.1057+11986_1057+11987insGA
ENST00000455470.5:c.1884-109_1884-108insGA
NM_001278055.1:c.1745-109_1745-108insGA	NP_001264984.1:n.1745-109_1745-108insGA
NM_014363.5:c.2186-109_2186-108insGA	NP_055178.3:n.2186-109_2186-108insGA
XM_005266338.1:c.2213-109_2213-108insGA	XP_005266395.1:n.2213-109_2213-108insGA
XM_011535038.1:c.2237-109_2237-108insGA	XP_011533340.1:n.2237-109_2237-108insGA
XM_011535039.1:c.2204-109_2204-108insGA	XP_011533341.1:n.2204-109_2204-108insGA
XM_005266338.2:c.2213-109_2213-108insGA	XP_005266395.1:n.2213-109_2213-108insGA
XM_011535039.2:c.2204-109_2204-108insGA	XP_011533341.1:n.2204-109_2204-108insGA
XM_017020539.1:c.2177-109_2177-108insGA	XP_016876028.1:n.2177-109_2177-108insGA
XM_024449337.1:c.2213-109_2213-108insGA	XP_024305105.1:n.2213-109_2213-108insGA
NM_014363.6:c.2186-109_2186-108insGA MANE Select	NP_055178.3:n.2186-109_2186-108insGA
NM_001278055.2:c.1745-109_1745-108insGA	NP_001264984.1:n.1745-109_1745-108insGA