Canonical Allele Identifier: CA387512029

Gene: SACS

Linked Data

• gnomAD v4: 13-23333356-G-T
• MyVariant Identifiers: chr13:g.23907495G>T (hg19) ; chr13:g.23333356G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333356G>T , CM000675.2:g.23333356G>T	GRCh38
NC_000013.10:g.23907495G>T , CM000675.1:g.23907495G>T	GRCh37
NC_000013.9:g.22805495G>T	NCBI36
NG_012342.1:g.105347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20429C>A	ENSP00000508399.1:n.2185+20429C>A
ENST00000682944.1:c.10547C>A	ENSP00000507173.1:p.Ala3516Asp
ENST00000683210.1:c.2185+20429C>A	ENSP00000506739.1:n.2185+20429C>A
ENST00000683270.1:c.6446-3872C>A	ENSP00000507624.1:n.6446-3872C>A
ENST00000683367.1:c.2177-3872C>A	ENSP00000507780.1:n.2177-3872C>A
ENST00000683489.1:c.2292-3404C>A	ENSP00000508403.1:n.2292-3404C>A
ENST00000683680.1:c.2319-3404C>A	ENSP00000507223.1:n.2319-3404C>A
ENST00000684163.1:c.2204-3872C>A	ENSP00000508262.1:n.2204-3872C>A
ENST00000684196.1:n.4543-3872C>A
ENST00000684325.1:c.2186-11682C>A	ENSP00000508121.1:n.2186-11682C>A
ENST00000684385.1:c.2221-3872C>A	ENSP00000507855.1:n.2221-3872C>A
ENST00000684497.1:c.2186-10712C>A	ENSP00000507057.1:n.2186-10712C>A
ENST00000382292.9:c.10520C>A MANE Select	ENSP00000371729.3:p.Ala3507Asp
ENST00000423156.2:c.2186-3872C>A	ENSP00000390925.2:n.2186-3872C>A
ENST00000455470.6:c.2432-3872C>A	ENSP00000406565.2:n.2432-3872C>A
ENST00000382292.7:c.10520C>A	ENSP00000371729.3:p.Ala3507Asp
ENST00000382298.7:c.10520C>A	ENSP00000371735.3:p.Ala3507Asp
ENST00000402364.1:c.8270C>A	ENSP00000385844.1:p.Ala2757Asp
ENST00000423156.1:c.1058-3872C>A	ENSP00000390925.1:n.1058-3872C>A
ENST00000455470.5:c.2130-3872C>A
NM_001278055.1:c.10079C>A	NP_001264984.1:p.Ala3360Asp
NM_014363.5:c.10520C>A	NP_055178.3:p.Ala3507Asp
XM_005266338.1:c.10547C>A	XP_005266395.1:p.Ala3516Asp
XM_011535038.1:c.10571C>A	XP_011533340.1:p.Ala3524Asp
XM_011535039.1:c.10538C>A	XP_011533341.1:p.Ala3513Asp
XM_005266338.2:c.10547C>A	XP_005266395.1:p.Ala3516Asp
XM_011535039.2:c.10538C>A	XP_011533341.1:p.Ala3513Asp
XM_017020539.1:c.10511C>A	XP_016876028.1:p.Ala3504Asp
XM_024449337.1:c.10547C>A	XP_024305105.1:p.Ala3516Asp
NM_014363.6:c.10520C>A MANE Select	NP_055178.3:p.Ala3507Asp
NM_001278055.2:c.10079C>A	NP_001264984.1:p.Ala3360Asp