Canonical Allele Identifier: CA387508851
Community Standard Title: NM_014363.6(SACS):c.11941C>T (p.Gln3981Ter)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23331935G>A , CM000675.2:g.23331935G>A GRCh38
NC_000013.10:g.23906074G>A , CM000675.1:g.23906074G>A GRCh37
NC_000013.9:g.22804074G>A NCBI36
NG_012342.1:g.106768C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.11941C>T MANE Select NP_055178.3:p.Gln3981Ter
ENST00000382292.9:c.11941C>T MANE Select ENSP00000371729.3:p.Gln3981Ter
NM_001278055.1:c.11500C>T NP_001264984.1:p.Gln3834Ter
NM_001278055.2:c.11500C>T NP_001264984.1:p.Gln3834Ter
NM_014363.5:c.11941C>T NP_055178.3:p.Gln3981Ter
ENST00000382292.7:c.11941C>T ENSP00000371729.3:p.Gln3981Ter
ENST00000382298.7:c.11941C>T ENSP00000371735.3:p.Gln3981Ter
ENST00000402364.1:c.9691C>T ENSP00000385844.1:p.Gln3231Ter
ENST00000423156.1:c.1058-2451C>T ENSP00000390925.1:n.1058-2451C>T
ENST00000423156.2:c.2186-2451C>T ENSP00000390925.2:n.2186-2451C>T
ENST00000455470.5:c.2130-2451C>T
ENST00000455470.6:c.2432-2451C>T ENSP00000406565.2:n.2432-2451C>T
ENST00000682775.1:c.2186-19820C>T ENSP00000508399.1:n.2186-19820C>T
ENST00000682944.1:c.11968C>T ENSP00000507173.1:p.Gln3990Ter
ENST00000683210.1:c.2185+21850C>T ENSP00000506739.1:n.2185+21850C>T
ENST00000683270.1:c.6446-2451C>T ENSP00000507624.1:n.6446-2451C>T
ENST00000683367.1:c.2177-2451C>T ENSP00000507780.1:n.2177-2451C>T
ENST00000683489.1:c.2292-1983C>T ENSP00000508403.1:n.2292-1983C>T
ENST00000683680.1:c.2319-1983C>T ENSP00000507223.1:n.2319-1983C>T
ENST00000684163.1:c.2204-2451C>T ENSP00000508262.1:n.2204-2451C>T
ENST00000684196.1:n.4543-2451C>T
ENST00000684325.1:c.2186-10261C>T ENSP00000508121.1:n.2186-10261C>T
ENST00000684385.1:c.2221-2451C>T ENSP00000507855.1:n.2221-2451C>T
ENST00000684497.1:c.2186-9291C>T ENSP00000507057.1:n.2186-9291C>T
XM_005266338.1:c.11968C>T XP_005266395.1:p.Gln3990Ter
XM_005266338.2:c.11968C>T XP_005266395.1:p.Gln3990Ter
XM_011535038.1:c.11992C>T XP_011533340.1:p.Gln3998Ter
XM_011535039.1:c.11959C>T XP_011533341.1:p.Gln3987Ter
XM_011535039.2:c.11959C>T XP_011533341.1:p.Gln3987Ter
XM_017020539.1:c.11932C>T XP_016876028.1:p.Gln3978Ter
XM_024449337.1:c.11968C>T XP_024305105.1:p.Gln3990Ter