Canonical Allele Identifier: CA16041649
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 370521
ClinVar RCV Id: RCV000410645
dbSNP Id: rs1057516554
MyVariant Identifiers: chr13:g.23915831T>C (hg19) chr13:g.23341692T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23341692T>C , CM000675.2:g.23341692T>C GRCh38
NC_000013.10:g.23915831T>C , CM000675.1:g.23915831T>C GRCh37
NC_000013.9:g.22813831T>C NCBI36
NG_012342.1:g.97011A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+12093A>G ENSP00000508399.1:n.2185+12093A>G
ENST00000682944.1:c.2213-2A>G ENSP00000507173.1:n.2213-2A>G
ENST00000683210.1:c.2185+12093A>G ENSP00000506739.1:n.2185+12093A>G
ENST00000683270.1:c.2177-2A>G ENSP00000507624.1:n.2177-2A>G
ENST00000683367.1:c.2176+12093A>G ENSP00000507780.1:n.2176+12093A>G
ENST00000683489.1:c.2186-2A>G ENSP00000508403.1:n.2186-2A>G
ENST00000683680.1:c.2213-2A>G ENSP00000507223.1:n.2213-2A>G
ENST00000684163.1:c.2203+5119A>G ENSP00000508262.1:n.2203+5119A>G
ENST00000684196.1:n.4542+12093A>G
ENST00000684325.1:c.2185+12093A>G ENSP00000508121.1:n.2185+12093A>G
ENST00000684385.1:c.2220+5119A>G ENSP00000507855.1:n.2220+5119A>G
ENST00000684497.1:c.2185+12093A>G ENSP00000507057.1:n.2185+12093A>G
ENST00000382292.9:c.2186-2A>G MANE Select ENSP00000371729.3:n.2186-2A>G
ENST00000423156.2:c.2185+12093A>G ENSP00000390925.2:n.2185+12093A>G
ENST00000455470.6:c.2186-2A>G ENSP00000406565.2:n.2186-2A>G
ENST00000382292.7:c.2186-2A>G ENSP00000371729.3:n.2186-2A>G
ENST00000382298.7:c.2186-2A>G ENSP00000371735.3:n.2186-2A>G
ENST00000402364.1:c.-65-2A>G ENSP00000385844.1:n.-65-2A>G
ENST00000423156.1:c.1057+12093A>G ENSP00000390925.1:n.1057+12093A>G
ENST00000455470.5:c.1884-2A>G
NM_001278055.1:c.1745-2A>G NP_001264984.1:n.1745-2A>G
NM_014363.5:c.2186-2A>G NP_055178.3:n.2186-2A>G
XM_005266338.1:c.2213-2A>G XP_005266395.1:n.2213-2A>G
XM_011535038.1:c.2237-2A>G XP_011533340.1:n.2237-2A>G
XM_011535039.1:c.2204-2A>G XP_011533341.1:n.2204-2A>G
XM_005266338.2:c.2213-2A>G XP_005266395.1:n.2213-2A>G
XM_011535039.2:c.2204-2A>G XP_011533341.1:n.2204-2A>G
XM_017020539.1:c.2177-2A>G XP_016876028.1:n.2177-2A>G
XM_024449337.1:c.2213-2A>G XP_024305105.1:n.2213-2A>G
NM_014363.6:c.2186-2A>G MANE Select NP_055178.3:n.2186-2A>G
NM_001278055.2:c.1745-2A>G NP_001264984.1:n.1745-2A>G
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