Canonical Allele Identifier: CA387518655
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23336267T>A , CM000675.2:g.23336267T>A GRCh38
NC_000013.10:g.23910406T>A , CM000675.1:g.23910406T>A GRCh37
NC_000013.9:g.22808406T>A NCBI36
NG_012342.1:g.102436A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+17518A>T ENSP00000508399.1:n.2185+17518A>T
ENST00000682944.1:c.7636A>T ENSP00000507173.1:p.Asn2546Tyr
ENST00000683210.1:c.2185+17518A>T ENSP00000506739.1:n.2185+17518A>T
ENST00000683270.1:c.6445+1155A>T ENSP00000507624.1:n.6445+1155A>T
ENST00000683367.1:c.2177-6783A>T ENSP00000507780.1:n.2177-6783A>T
ENST00000683489.1:c.2291+5318A>T ENSP00000508403.1:n.2291+5318A>T
ENST00000683680.1:c.2318+5318A>T ENSP00000507223.1:n.2318+5318A>T
ENST00000684163.1:c.2204-6783A>T ENSP00000508262.1:n.2204-6783A>T
ENST00000684196.1:n.4543-6783A>T
ENST00000684325.1:c.2186-14593A>T ENSP00000508121.1:n.2186-14593A>T
ENST00000684385.1:c.2221-6783A>T ENSP00000507855.1:n.2221-6783A>T
ENST00000684497.1:c.2186-13623A>T ENSP00000507057.1:n.2186-13623A>T
ENST00000382292.9:c.7609A>T MANE Select ENSP00000371729.3:p.Asn2537Tyr
ENST00000423156.2:c.2186-6783A>T ENSP00000390925.2:n.2186-6783A>T
ENST00000455470.6:c.2431+5178A>T ENSP00000406565.2:n.2431+5178A>T
ENST00000382292.7:c.7609A>T ENSP00000371729.3:p.Asn2537Tyr
ENST00000382298.7:c.7609A>T ENSP00000371735.3:p.Asn2537Tyr
ENST00000402364.1:c.5359A>T ENSP00000385844.1:p.Asn1787Tyr
ENST00000423156.1:c.1058-6783A>T ENSP00000390925.1:n.1058-6783A>T
ENST00000455470.5:c.2129+5178A>T
NM_001278055.1:c.7168A>T NP_001264984.1:p.Asn2390Tyr
NM_014363.5:c.7609A>T NP_055178.3:p.Asn2537Tyr
XM_005266338.1:c.7636A>T XP_005266395.1:p.Asn2546Tyr
XM_011535038.1:c.7660A>T XP_011533340.1:p.Asn2554Tyr
XM_011535039.1:c.7627A>T XP_011533341.1:p.Asn2543Tyr
XM_005266338.2:c.7636A>T XP_005266395.1:p.Asn2546Tyr
XM_011535039.2:c.7627A>T XP_011533341.1:p.Asn2543Tyr
XM_017020539.1:c.7600A>T XP_016876028.1:p.Asn2534Tyr
XM_024449337.1:c.7636A>T XP_024305105.1:p.Asn2546Tyr
NM_014363.6:c.7609A>T MANE Select NP_055178.3:p.Asn2537Tyr
NM_001278055.2:c.7168A>T NP_001264984.1:p.Asn2390Tyr