Canonical Allele Identifier: CA387512819

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907848C>A (hg19) ; chr13:g.23333709C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333709C>A , CM000675.2:g.23333709C>A	GRCh38
NC_000013.10:g.23907848C>A , CM000675.1:g.23907848C>A	GRCh37
NC_000013.9:g.22805848C>A	NCBI36
NG_012342.1:g.104994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20076G>T	ENSP00000508399.1:n.2185+20076G>T
ENST00000682944.1:c.10194G>T	ENSP00000507173.1:p.Met3398Ile
ENST00000683210.1:c.2185+20076G>T	ENSP00000506739.1:n.2185+20076G>T
ENST00000683270.1:c.6445+3713G>T	ENSP00000507624.1:n.6445+3713G>T
ENST00000683367.1:c.2177-4225G>T	ENSP00000507780.1:n.2177-4225G>T
ENST00000683489.1:c.2292-3757G>T	ENSP00000508403.1:n.2292-3757G>T
ENST00000683680.1:c.2319-3757G>T	ENSP00000507223.1:n.2319-3757G>T
ENST00000684163.1:c.2204-4225G>T	ENSP00000508262.1:n.2204-4225G>T
ENST00000684196.1:n.4543-4225G>T
ENST00000684325.1:c.2186-12035G>T	ENSP00000508121.1:n.2186-12035G>T
ENST00000684385.1:c.2221-4225G>T	ENSP00000507855.1:n.2221-4225G>T
ENST00000684497.1:c.2186-11065G>T	ENSP00000507057.1:n.2186-11065G>T
ENST00000382292.9:c.10167G>T MANE Select	ENSP00000371729.3:p.Met3389Ile
ENST00000423156.2:c.2186-4225G>T	ENSP00000390925.2:n.2186-4225G>T
ENST00000455470.6:c.2432-4225G>T	ENSP00000406565.2:n.2432-4225G>T
ENST00000382292.7:c.10167G>T	ENSP00000371729.3:p.Met3389Ile
ENST00000382298.7:c.10167G>T	ENSP00000371735.3:p.Met3389Ile
ENST00000402364.1:c.7917G>T	ENSP00000385844.1:p.Met2639Ile
ENST00000423156.1:c.1058-4225G>T	ENSP00000390925.1:n.1058-4225G>T
ENST00000455470.5:c.2130-4225G>T
NM_001278055.1:c.9726G>T	NP_001264984.1:p.Met3242Ile
NM_014363.5:c.10167G>T	NP_055178.3:p.Met3389Ile
XM_005266338.1:c.10194G>T	XP_005266395.1:p.Met3398Ile
XM_011535038.1:c.10218G>T	XP_011533340.1:p.Met3406Ile
XM_011535039.1:c.10185G>T	XP_011533341.1:p.Met3395Ile
XM_005266338.2:c.10194G>T	XP_005266395.1:p.Met3398Ile
XM_011535039.2:c.10185G>T	XP_011533341.1:p.Met3395Ile
XM_017020539.1:c.10158G>T	XP_016876028.1:p.Met3386Ile
XM_024449337.1:c.10194G>T	XP_024305105.1:p.Met3398Ile
NM_014363.6:c.10167G>T MANE Select	NP_055178.3:p.Met3389Ile
NM_001278055.2:c.9726G>T	NP_001264984.1:p.Met3242Ile