Canonical Allele Identifier: CA387504718

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23904334T>C (hg19) ; chr13:g.23330195T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330195T>C , CM000675.2:g.23330195T>C	GRCh38
NC_000013.10:g.23904334T>C , CM000675.1:g.23904334T>C	GRCh37
NC_000013.9:g.22802334T>C	NCBI36
NG_012342.1:g.108508A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18080A>G	ENSP00000508399.1:n.2186-18080A>G
ENST00000682944.1:c.13708A>G	ENSP00000507173.1:p.Met4570Val
ENST00000683210.1:c.2185+23590A>G	ENSP00000506739.1:n.2185+23590A>G
ENST00000683270.1:c.6446-711A>G	ENSP00000507624.1:n.6446-711A>G
ENST00000683367.1:c.2177-711A>G	ENSP00000507780.1:n.2177-711A>G
ENST00000683489.1:c.2292-243A>G	ENSP00000508403.1:n.2292-243A>G
ENST00000683680.1:c.2319-243A>G	ENSP00000507223.1:n.2319-243A>G
ENST00000684163.1:c.2204-711A>G	ENSP00000508262.1:n.2204-711A>G
ENST00000684196.1:n.4543-711A>G
ENST00000684325.1:c.2186-8521A>G	ENSP00000508121.1:n.2186-8521A>G
ENST00000684385.1:c.2221-711A>G	ENSP00000507855.1:n.2221-711A>G
ENST00000684497.1:c.2186-7551A>G	ENSP00000507057.1:n.2186-7551A>G
ENST00000382292.9:c.13681A>G MANE Select	ENSP00000371729.3:p.Met4561Val
ENST00000423156.2:c.2186-711A>G	ENSP00000390925.2:n.2186-711A>G
ENST00000455470.6:c.2432-711A>G	ENSP00000406565.2:n.2432-711A>G
ENST00000382292.7:c.13681A>G	ENSP00000371729.3:p.Met4561Val
ENST00000382298.7:c.13681A>G	ENSP00000371735.3:p.Met4561Val
ENST00000402364.1:c.11431A>G	ENSP00000385844.1:p.Met3811Val
ENST00000423156.1:c.1058-711A>G	ENSP00000390925.1:n.1058-711A>G
ENST00000455470.5:c.2130-711A>G
NM_001278055.1:c.13240A>G	NP_001264984.1:p.Met4414Val
NM_014363.5:c.13681A>G	NP_055178.3:p.Met4561Val
XM_005266338.1:c.13708A>G	XP_005266395.1:p.Met4570Val
XM_011535038.1:c.13732A>G	XP_011533340.1:p.Met4578Val
XM_011535039.1:c.13699A>G	XP_011533341.1:p.Met4567Val
XM_005266338.2:c.13708A>G	XP_005266395.1:p.Met4570Val
XM_011535039.2:c.13699A>G	XP_011533341.1:p.Met4567Val
XM_017020539.1:c.13672A>G	XP_016876028.1:p.Met4558Val
XM_024449337.1:c.13708A>G	XP_024305105.1:p.Met4570Val
NM_014363.6:c.13681A>G MANE Select	NP_055178.3:p.Met4561Val
NM_001278055.2:c.13240A>G	NP_001264984.1:p.Met4414Val