Canonical Allele Identifier: CA387549774

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23929539A>T (hg19) ; chr13:g.23355400A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23355400A>T , CM000675.2:g.23355400A>T	GRCh38
NC_000013.10:g.23929539A>T , CM000675.1:g.23929539A>T	GRCh37
NC_000013.9:g.22827539A>T	NCBI36
NG_012342.1:g.83303T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.1212T>A	ENSP00000508399.1:p.Ser404Arg
ENST00000682944.1:c.1212T>A	ENSP00000507173.1:p.Ser404Arg
ENST00000683154.1:n.1350T>A
ENST00000683210.1:c.1212T>A	ENSP00000506739.1:p.Ser404Arg
ENST00000683270.1:c.1203T>A	ENSP00000507624.1:p.Ser401Arg
ENST00000683367.1:c.1203T>A	ENSP00000507780.1:p.Ser401Arg
ENST00000683489.1:c.1212T>A	ENSP00000508403.1:p.Ser404Arg
ENST00000683680.1:c.1212T>A	ENSP00000507223.1:p.Ser404Arg
ENST00000684163.1:c.1203T>A	ENSP00000508262.1:p.Ser401Arg
ENST00000684196.1:n.3569T>A
ENST00000684325.1:c.1212T>A	ENSP00000508121.1:p.Ser404Arg
ENST00000684385.1:c.1212T>A	ENSP00000507855.1:p.Ser404Arg
ENST00000684497.1:c.1212T>A	ENSP00000507057.1:p.Ser404Arg
ENST00000382292.9:c.1212T>A MANE Select	ENSP00000371729.3:p.Ser404Arg
ENST00000423156.2:c.1212T>A	ENSP00000390925.2:p.Ser404Arg
ENST00000455470.6:c.1212T>A	ENSP00000406565.2:p.Ser404Arg
ENST00000382292.7:c.1212T>A	ENSP00000371729.3:p.Ser404Arg
ENST00000382298.7:c.1212T>A	ENSP00000371735.3:p.Ser404Arg
ENST00000402364.1:c.-1039T>A	ENSP00000385844.1:n.-1039T>A
ENST00000423156.1:c.84T>A	ENSP00000390925.1:p.Ser28Arg
ENST00000455470.5:c.910T>A
NM_001278055.1:c.771T>A	NP_001264984.1:p.Ser257Arg
NM_014363.5:c.1212T>A	NP_055178.3:p.Ser404Arg
XM_005266338.1:c.1212T>A	XP_005266395.1:p.Ser404Arg
XM_011535038.1:c.1236T>A	XP_011533340.1:p.Ser412Arg
XM_011535039.1:c.1203T>A	XP_011533341.1:p.Ser401Arg
XM_005266338.2:c.1212T>A	XP_005266395.1:p.Ser404Arg
XM_011535039.2:c.1203T>A	XP_011533341.1:p.Ser401Arg
XM_017020539.1:c.1203T>A	XP_016876028.1:p.Ser401Arg
XM_024449337.1:c.1212T>A	XP_024305105.1:p.Ser404Arg
NM_014363.6:c.1212T>A MANE Select	NP_055178.3:p.Ser404Arg
NM_001278055.2:c.771T>A	NP_001264984.1:p.Ser257Arg