Canonical Allele Identifier: CA2078645424

Gene: SACS

Linked Data

• dbSNP Id: rs1869268363

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341847_23341850del , CM000675.2:g.23341847_23341850del	GRCh38
NC_000013.10:g.23915986_23915989del , CM000675.1:g.23915986_23915989del	GRCh37
NC_000013.9:g.22813986_22813989del	NCBI36
NG_012342.1:g.96853_96856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+11935_2185+11938del	ENSP00000508399.1:n.2185+11935_2185+11938del
ENST00000682944.1:c.2213-160_2213-157del	ENSP00000507173.1:n.2213-160_2213-157del
ENST00000683210.1:c.2185+11935_2185+11938del	ENSP00000506739.1:n.2185+11935_2185+11938del
ENST00000683270.1:c.2177-160_2177-157del	ENSP00000507624.1:n.2177-160_2177-157del
ENST00000683367.1:c.2176+11935_2176+11938del	ENSP00000507780.1:n.2176+11935_2176+11938del
ENST00000683489.1:c.2186-160_2186-157del	ENSP00000508403.1:n.2186-160_2186-157del
ENST00000683680.1:c.2213-160_2213-157del	ENSP00000507223.1:n.2213-160_2213-157del
ENST00000684163.1:c.2203+4961_2203+4964del	ENSP00000508262.1:n.2203+4961_2203+4964del
ENST00000684196.1:n.4542+11935_4542+11938del
ENST00000684325.1:c.2185+11935_2185+11938del	ENSP00000508121.1:n.2185+11935_2185+11938del
ENST00000684385.1:c.2220+4961_2220+4964del	ENSP00000507855.1:n.2220+4961_2220+4964del
ENST00000684497.1:c.2185+11935_2185+11938del	ENSP00000507057.1:n.2185+11935_2185+11938del
ENST00000382292.9:c.2186-160_2186-157del MANE Select	ENSP00000371729.3:n.2186-160_2186-157del
ENST00000423156.2:c.2185+11935_2185+11938del	ENSP00000390925.2:n.2185+11935_2185+11938del
ENST00000455470.6:c.2186-160_2186-157del	ENSP00000406565.2:n.2186-160_2186-157del
ENST00000382292.7:c.2186-160_2186-157del	ENSP00000371729.3:n.2186-160_2186-157del
ENST00000382298.7:c.2186-160_2186-157del	ENSP00000371735.3:n.2186-160_2186-157del
ENST00000402364.1:c.-65-160_-65-157del	ENSP00000385844.1:n.-65-160_-65-157del
ENST00000423156.1:c.1057+11935_1057+11938del	ENSP00000390925.1:n.1057+11935_1057+11938del
ENST00000455470.5:c.1884-160_1884-157del
NM_001278055.1:c.1745-160_1745-157del	NP_001264984.1:n.1745-160_1745-157del
NM_014363.5:c.2186-160_2186-157del	NP_055178.3:n.2186-160_2186-157del
XM_005266338.1:c.2213-160_2213-157del	XP_005266395.1:n.2213-160_2213-157del
XM_011535038.1:c.2237-160_2237-157del	XP_011533340.1:n.2237-160_2237-157del
XM_011535039.1:c.2204-160_2204-157del	XP_011533341.1:n.2204-160_2204-157del
XM_005266338.2:c.2213-160_2213-157del	XP_005266395.1:n.2213-160_2213-157del
XM_011535039.2:c.2204-160_2204-157del	XP_011533341.1:n.2204-160_2204-157del
XM_017020539.1:c.2177-160_2177-157del	XP_016876028.1:n.2177-160_2177-157del
XM_024449337.1:c.2213-160_2213-157del	XP_024305105.1:n.2213-160_2213-157del
NM_014363.6:c.2186-160_2186-157del MANE Select	NP_055178.3:n.2186-160_2186-157del
NM_001278055.2:c.1745-160_1745-157del	NP_001264984.1:n.1745-160_1745-157del