Canonical Allele Identifier: CA6910244
Community Standard Title: NM_014363.6(SACS):c.11665C>T (p.Gln3889Ter)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23332211G>A , CM000675.2:g.23332211G>A GRCh38
NC_000013.10:g.23906350G>A , CM000675.1:g.23906350G>A GRCh37
NC_000013.9:g.22804350G>A NCBI36
NG_012342.1:g.106492C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.11665C>T MANE Select NP_055178.3:p.Gln3889Ter
ENST00000382292.9:c.11665C>T MANE Select ENSP00000371729.3:p.Gln3889Ter
NM_001278055.1:c.11224C>T NP_001264984.1:p.Gln3742Ter
NM_001278055.2:c.11224C>T NP_001264984.1:p.Gln3742Ter
NM_014363.5:c.11665C>T NP_055178.3:p.Gln3889Ter
ENST00000382292.7:c.11665C>T ENSP00000371729.3:p.Gln3889Ter
ENST00000382298.7:c.11665C>T ENSP00000371735.3:p.Gln3889Ter
ENST00000402364.1:c.9415C>T ENSP00000385844.1:p.Gln3139Ter
ENST00000423156.1:c.1058-2727C>T ENSP00000390925.1:n.1058-2727C>T
ENST00000423156.2:c.2186-2727C>T ENSP00000390925.2:n.2186-2727C>T
ENST00000455470.5:c.2130-2727C>T
ENST00000455470.6:c.2432-2727C>T ENSP00000406565.2:n.2432-2727C>T
ENST00000682775.1:c.2186-20096C>T ENSP00000508399.1:n.2186-20096C>T
ENST00000682944.1:c.11692C>T ENSP00000507173.1:p.Gln3898Ter
ENST00000683210.1:c.2185+21574C>T ENSP00000506739.1:n.2185+21574C>T
ENST00000683270.1:c.6446-2727C>T ENSP00000507624.1:n.6446-2727C>T
ENST00000683367.1:c.2177-2727C>T ENSP00000507780.1:n.2177-2727C>T
ENST00000683489.1:c.2292-2259C>T ENSP00000508403.1:n.2292-2259C>T
ENST00000683680.1:c.2319-2259C>T ENSP00000507223.1:n.2319-2259C>T
ENST00000684163.1:c.2204-2727C>T ENSP00000508262.1:n.2204-2727C>T
ENST00000684196.1:n.4543-2727C>T
ENST00000684325.1:c.2186-10537C>T ENSP00000508121.1:n.2186-10537C>T
ENST00000684385.1:c.2221-2727C>T ENSP00000507855.1:n.2221-2727C>T
ENST00000684497.1:c.2186-9567C>T ENSP00000507057.1:n.2186-9567C>T
XM_005266338.1:c.11692C>T XP_005266395.1:p.Gln3898Ter
XM_005266338.2:c.11692C>T XP_005266395.1:p.Gln3898Ter
XM_011535038.1:c.11716C>T XP_011533340.1:p.Gln3906Ter
XM_011535039.1:c.11683C>T XP_011533341.1:p.Gln3895Ter
XM_011535039.2:c.11683C>T XP_011533341.1:p.Gln3895Ter
XM_017020539.1:c.11656C>T XP_016876028.1:p.Gln3886Ter
XM_024449337.1:c.11692C>T XP_024305105.1:p.Gln3898Ter