Canonical Allele Identifier: CA483158879
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23908019A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333880A>C , CM000675.2:g.23333880A>C GRCh38
NC_000013.10:g.23908019A>C , CM000675.1:g.23908019A>C GRCh37
NC_000013.9:g.22806019A>C NCBI36
NG_012342.1:g.104823T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+19905T>G ENSP00000508399.1:n.2185+19905T>G
ENST00000682944.1:c.10023T>G ENSP00000507173.1:p.Leu3341=
ENST00000683210.1:c.2185+19905T>G ENSP00000506739.1:n.2185+19905T>G
ENST00000683270.1:c.6445+3542T>G ENSP00000507624.1:n.6445+3542T>G
ENST00000683367.1:c.2177-4396T>G ENSP00000507780.1:n.2177-4396T>G
ENST00000683489.1:c.2292-3928T>G ENSP00000508403.1:n.2292-3928T>G
ENST00000683680.1:c.2319-3928T>G ENSP00000507223.1:n.2319-3928T>G
ENST00000684163.1:c.2204-4396T>G ENSP00000508262.1:n.2204-4396T>G
ENST00000684196.1:n.4543-4396T>G
ENST00000684325.1:c.2186-12206T>G ENSP00000508121.1:n.2186-12206T>G
ENST00000684385.1:c.2221-4396T>G ENSP00000507855.1:n.2221-4396T>G
ENST00000684497.1:c.2186-11236T>G ENSP00000507057.1:n.2186-11236T>G
ENST00000382292.9:c.9996T>G MANE Select ENSP00000371729.3:p.Leu3332=
ENST00000423156.2:c.2186-4396T>G ENSP00000390925.2:n.2186-4396T>G
ENST00000455470.6:c.2432-4396T>G ENSP00000406565.2:n.2432-4396T>G
ENST00000382292.7:c.9996T>G ENSP00000371729.3:p.Leu3332=
ENST00000382298.7:c.9996T>G ENSP00000371735.3:p.Leu3332=
ENST00000402364.1:c.7746T>G ENSP00000385844.1:p.Leu2582=
ENST00000423156.1:c.1058-4396T>G ENSP00000390925.1:n.1058-4396T>G
ENST00000455470.5:c.2130-4396T>G
NM_001278055.1:c.9555T>G NP_001264984.1:p.Leu3185=
NM_014363.5:c.9996T>G NP_055178.3:p.Leu3332=
XM_005266338.1:c.10023T>G XP_005266395.1:p.Leu3341=
XM_011535038.1:c.10047T>G XP_011533340.1:p.Leu3349=
XM_011535039.1:c.10014T>G XP_011533341.1:p.Leu3338=
XM_005266338.2:c.10023T>G XP_005266395.1:p.Leu3341=
XM_011535039.2:c.10014T>G XP_011533341.1:p.Leu3338=
XM_017020539.1:c.9987T>G XP_016876028.1:p.Leu3329=
XM_024449337.1:c.10023T>G XP_024305105.1:p.Leu3341=
NM_014363.6:c.9996T>G MANE Select NP_055178.3:p.Leu3332=
NM_001278055.2:c.9555T>G NP_001264984.1:p.Leu3185=