Canonical Allele Identifier: CA387520849
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337140A>T , CM000675.2:g.23337140A>T GRCh38
NC_000013.10:g.23911279A>T , CM000675.1:g.23911279A>T GRCh37
NC_000013.9:g.22809279A>T NCBI36
NG_012342.1:g.101563T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+16645T>A ENSP00000508399.1:n.2185+16645T>A
ENST00000682944.1:c.6763T>A ENSP00000507173.1:p.Tyr2255Asn
ENST00000683210.1:c.2185+16645T>A ENSP00000506739.1:n.2185+16645T>A
ENST00000683270.1:c.6445+282T>A ENSP00000507624.1:n.6445+282T>A
ENST00000683367.1:c.2177-7656T>A ENSP00000507780.1:n.2177-7656T>A
ENST00000683489.1:c.2291+4445T>A ENSP00000508403.1:n.2291+4445T>A
ENST00000683680.1:c.2318+4445T>A ENSP00000507223.1:n.2318+4445T>A
ENST00000684163.1:c.2204-7656T>A ENSP00000508262.1:n.2204-7656T>A
ENST00000684196.1:n.4543-7656T>A
ENST00000684325.1:c.2186-15466T>A ENSP00000508121.1:n.2186-15466T>A
ENST00000684385.1:c.2221-7656T>A ENSP00000507855.1:n.2221-7656T>A
ENST00000684497.1:c.2186-14496T>A ENSP00000507057.1:n.2186-14496T>A
ENST00000382292.9:c.6736T>A MANE Select ENSP00000371729.3:p.Tyr2246Asn
ENST00000423156.2:c.2186-7656T>A ENSP00000390925.2:n.2186-7656T>A
ENST00000455470.6:c.2431+4305T>A ENSP00000406565.2:n.2431+4305T>A
ENST00000382292.7:c.6736T>A ENSP00000371729.3:p.Tyr2246Asn
ENST00000382298.7:c.6736T>A ENSP00000371735.3:p.Tyr2246Asn
ENST00000402364.1:c.4486T>A ENSP00000385844.1:p.Tyr1496Asn
ENST00000423156.1:c.1058-7656T>A ENSP00000390925.1:n.1058-7656T>A
ENST00000455470.5:c.2129+4305T>A
NM_001278055.1:c.6295T>A NP_001264984.1:p.Tyr2099Asn
NM_014363.5:c.6736T>A NP_055178.3:p.Tyr2246Asn
XM_005266338.1:c.6763T>A XP_005266395.1:p.Tyr2255Asn
XM_011535038.1:c.6787T>A XP_011533340.1:p.Tyr2263Asn
XM_011535039.1:c.6754T>A XP_011533341.1:p.Tyr2252Asn
XM_005266338.2:c.6763T>A XP_005266395.1:p.Tyr2255Asn
XM_011535039.2:c.6754T>A XP_011533341.1:p.Tyr2252Asn
XM_017020539.1:c.6727T>A XP_016876028.1:p.Tyr2243Asn
XM_024449337.1:c.6763T>A XP_024305105.1:p.Tyr2255Asn
NM_014363.6:c.6736T>A MANE Select NP_055178.3:p.Tyr2246Asn
NM_001278055.2:c.6295T>A NP_001264984.1:p.Tyr2099Asn