Canonical Allele Identifier: CA387512145

Gene: SACS

Linked Data

• dbSNP Id: rs755590920
• MyVariant Identifiers: chr13:g.23907545A>C (hg19) ; chr13:g.23333406A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333406A>C , CM000675.2:g.23333406A>C	GRCh38
NC_000013.10:g.23907545A>C , CM000675.1:g.23907545A>C	GRCh37
NC_000013.9:g.22805545A>C	NCBI36
NG_012342.1:g.105297T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20379T>G	ENSP00000508399.1:n.2185+20379T>G
ENST00000682944.1:c.10497T>G	ENSP00000507173.1:p.Tyr3499Ter
ENST00000683210.1:c.2185+20379T>G	ENSP00000506739.1:n.2185+20379T>G
ENST00000683270.1:c.6446-3922T>G	ENSP00000507624.1:n.6446-3922T>G
ENST00000683367.1:c.2177-3922T>G	ENSP00000507780.1:n.2177-3922T>G
ENST00000683489.1:c.2292-3454T>G	ENSP00000508403.1:n.2292-3454T>G
ENST00000683680.1:c.2319-3454T>G	ENSP00000507223.1:n.2319-3454T>G
ENST00000684163.1:c.2204-3922T>G	ENSP00000508262.1:n.2204-3922T>G
ENST00000684196.1:n.4543-3922T>G
ENST00000684325.1:c.2186-11732T>G	ENSP00000508121.1:n.2186-11732T>G
ENST00000684385.1:c.2221-3922T>G	ENSP00000507855.1:n.2221-3922T>G
ENST00000684497.1:c.2186-10762T>G	ENSP00000507057.1:n.2186-10762T>G
ENST00000382292.9:c.10470T>G MANE Select	ENSP00000371729.3:p.Tyr3490Ter
ENST00000423156.2:c.2186-3922T>G	ENSP00000390925.2:n.2186-3922T>G
ENST00000455470.6:c.2432-3922T>G	ENSP00000406565.2:n.2432-3922T>G
ENST00000382292.7:c.10470T>G	ENSP00000371729.3:p.Tyr3490Ter
ENST00000382298.7:c.10470T>G	ENSP00000371735.3:p.Tyr3490Ter
ENST00000402364.1:c.8220T>G	ENSP00000385844.1:p.Tyr2740Ter
ENST00000423156.1:c.1058-3922T>G	ENSP00000390925.1:n.1058-3922T>G
ENST00000455470.5:c.2130-3922T>G
NM_001278055.1:c.10029T>G	NP_001264984.1:p.Tyr3343Ter
NM_014363.5:c.10470T>G	NP_055178.3:p.Tyr3490Ter
XM_005266338.1:c.10497T>G	XP_005266395.1:p.Tyr3499Ter
XM_011535038.1:c.10521T>G	XP_011533340.1:p.Tyr3507Ter
XM_011535039.1:c.10488T>G	XP_011533341.1:p.Tyr3496Ter
XM_005266338.2:c.10497T>G	XP_005266395.1:p.Tyr3499Ter
XM_011535039.2:c.10488T>G	XP_011533341.1:p.Tyr3496Ter
XM_017020539.1:c.10461T>G	XP_016876028.1:p.Tyr3487Ter
XM_024449337.1:c.10497T>G	XP_024305105.1:p.Tyr3499Ter
NM_014363.6:c.10470T>G MANE Select	NP_055178.3:p.Tyr3490Ter
NM_001278055.2:c.10029T>G	NP_001264984.1:p.Tyr3343Ter