Canonical Allele Identifier: CA482922455

Gene: SACS

Linked Data

• COSMIC: COSM4896408 ; COSM4896409
• MyVariant Identifiers: chr13:g.23932610G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23358471G>A , CM000675.2:g.23358471G>A	GRCh38
NC_000013.10:g.23932610G>A , CM000675.1:g.23932610G>A	GRCh37
NC_000013.9:g.22830610G>A	NCBI36
NG_012342.1:g.80232C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.468C>T	ENSP00000508399.1:p.Leu156=
ENST00000682944.1:c.468C>T	ENSP00000507173.1:p.Leu156=
ENST00000683154.1:n.606C>T
ENST00000683210.1:c.468C>T	ENSP00000506739.1:p.Leu156=
ENST00000683270.1:c.459C>T	ENSP00000507624.1:p.Leu153=
ENST00000683367.1:c.459C>T	ENSP00000507780.1:p.Leu153=
ENST00000683489.1:c.468C>T	ENSP00000508403.1:p.Leu156=
ENST00000683680.1:c.468C>T	ENSP00000507223.1:p.Leu156=
ENST00000684163.1:c.459C>T	ENSP00000508262.1:p.Leu153=
ENST00000684196.1:n.2825C>T
ENST00000684325.1:c.468C>T	ENSP00000508121.1:p.Leu156=
ENST00000684385.1:c.468C>T	ENSP00000507855.1:p.Leu156=
ENST00000684497.1:c.468C>T	ENSP00000507057.1:p.Leu156=
ENST00000382292.9:c.468C>T MANE Select	ENSP00000371729.3:p.Leu156=
ENST00000423156.2:c.468C>T	ENSP00000390925.2:p.Leu156=
ENST00000455470.6:c.468C>T	ENSP00000406565.2:p.Leu156=
ENST00000382292.7:c.468C>T	ENSP00000371729.3:p.Leu156=
ENST00000382298.7:c.468C>T	ENSP00000371735.3:p.Leu156=
ENST00000402364.1:c.-1783C>T	ENSP00000385844.1:n.-1783C>T
ENST00000455470.5:c.166C>T
NM_001278055.1:c.27C>T	NP_001264984.1:p.Leu9=
NM_014363.5:c.468C>T	NP_055178.3:p.Leu156=
XM_005266338.1:c.468C>T	XP_005266395.1:p.Leu156=
XM_011535038.1:c.492C>T	XP_011533340.1:p.Leu164=
XM_011535039.1:c.459C>T	XP_011533341.1:p.Leu153=
XM_005266338.2:c.468C>T	XP_005266395.1:p.Leu156=
XM_011535039.2:c.459C>T	XP_011533341.1:p.Leu153=
XM_017020539.1:c.459C>T	XP_016876028.1:p.Leu153=
XM_024449337.1:c.468C>T	XP_024305105.1:p.Leu156=
NM_014363.6:c.468C>T MANE Select	NP_055178.3:p.Leu156=
NM_001278055.2:c.27C>T	NP_001264984.1:p.Leu9=