Canonical Allele Identifier: CA387546326
Community Standard Title: NM_014363.6(SACS):c.1814C>T (p.Pro605Leu)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23354798G>A , CM000675.2:g.23354798G>A GRCh38
NC_000013.10:g.23928937G>A , CM000675.1:g.23928937G>A GRCh37
NC_000013.9:g.22826937G>A NCBI36
NG_012342.1:g.83905C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.1814C>T MANE Select NP_055178.3:p.Pro605Leu
ENST00000382292.9:c.1814C>T MANE Select ENSP00000371729.3:p.Pro605Leu
NM_001278055.1:c.1373C>T NP_001264984.1:p.Pro458Leu
NM_001278055.2:c.1373C>T NP_001264984.1:p.Pro458Leu
NM_014363.5:c.1814C>T NP_055178.3:p.Pro605Leu
ENST00000382292.7:c.1814C>T ENSP00000371729.3:p.Pro605Leu
ENST00000382298.7:c.1814C>T ENSP00000371735.3:p.Pro605Leu
ENST00000402364.1:c.-437C>T ENSP00000385844.1:n.-437C>T
ENST00000423156.1:c.686C>T ENSP00000390925.1:p.Pro229Leu
ENST00000423156.2:c.1814C>T ENSP00000390925.2:p.Pro605Leu
ENST00000455470.5:c.1512C>T
ENST00000455470.6:c.1814C>T ENSP00000406565.2:p.Pro605Leu
ENST00000476776.1:n.93C>T
ENST00000682775.1:c.1814C>T ENSP00000508399.1:p.Pro605Leu
ENST00000682944.1:c.1814C>T ENSP00000507173.1:p.Pro605Leu
ENST00000683154.1:n.1952C>T
ENST00000683210.1:c.1814C>T ENSP00000506739.1:p.Pro605Leu
ENST00000683270.1:c.1805C>T ENSP00000507624.1:p.Pro602Leu
ENST00000683367.1:c.1805C>T ENSP00000507780.1:p.Pro602Leu
ENST00000683489.1:c.1814C>T ENSP00000508403.1:p.Pro605Leu
ENST00000683680.1:c.1814C>T ENSP00000507223.1:p.Pro605Leu
ENST00000684163.1:c.1805C>T ENSP00000508262.1:p.Pro602Leu
ENST00000684196.1:n.4171C>T
ENST00000684325.1:c.1814C>T ENSP00000508121.1:p.Pro605Leu
ENST00000684385.1:c.1814C>T ENSP00000507855.1:p.Pro605Leu
ENST00000684497.1:c.1814C>T ENSP00000507057.1:p.Pro605Leu
XM_005266338.1:c.1814C>T XP_005266395.1:p.Pro605Leu
XM_005266338.2:c.1814C>T XP_005266395.1:p.Pro605Leu
XM_011535038.1:c.1838C>T XP_011533340.1:p.Pro613Leu
XM_011535039.1:c.1805C>T XP_011533341.1:p.Pro602Leu
XM_011535039.2:c.1805C>T XP_011533341.1:p.Pro602Leu
XM_017020539.1:c.1805C>T XP_016876028.1:p.Pro602Leu
XM_024449337.1:c.1814C>T XP_024305105.1:p.Pro605Leu