Canonical Allele Identifier: CA387551949

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23932511T>G (hg19) ; chr13:g.23358372T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23358372T>G , CM000675.2:g.23358372T>G	GRCh38
NC_000013.10:g.23932511T>G , CM000675.1:g.23932511T>G	GRCh37
NC_000013.9:g.22830511T>G	NCBI36
NG_012342.1:g.80331A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.567A>C	ENSP00000508399.1:p.Arg189Ser
ENST00000682944.1:c.567A>C	ENSP00000507173.1:p.Arg189Ser
ENST00000683154.1:n.705A>C
ENST00000683210.1:c.567A>C	ENSP00000506739.1:p.Arg189Ser
ENST00000683270.1:c.558A>C	ENSP00000507624.1:p.Arg186Ser
ENST00000683367.1:c.558A>C	ENSP00000507780.1:p.Arg186Ser
ENST00000683489.1:c.567A>C	ENSP00000508403.1:p.Arg189Ser
ENST00000683680.1:c.567A>C	ENSP00000507223.1:p.Arg189Ser
ENST00000684163.1:c.558A>C	ENSP00000508262.1:p.Arg186Ser
ENST00000684196.1:n.2924A>C
ENST00000684325.1:c.567A>C	ENSP00000508121.1:p.Arg189Ser
ENST00000684385.1:c.567A>C	ENSP00000507855.1:p.Arg189Ser
ENST00000684497.1:c.567A>C	ENSP00000507057.1:p.Arg189Ser
ENST00000382292.9:c.567A>C MANE Select	ENSP00000371729.3:p.Arg189Ser
ENST00000423156.2:c.567A>C	ENSP00000390925.2:p.Arg189Ser
ENST00000455470.6:c.567A>C	ENSP00000406565.2:p.Arg189Ser
ENST00000382292.7:c.567A>C	ENSP00000371729.3:p.Arg189Ser
ENST00000382298.7:c.567A>C	ENSP00000371735.3:p.Arg189Ser
ENST00000402364.1:c.-1684A>C	ENSP00000385844.1:n.-1684A>C
ENST00000455470.5:c.265A>C
NM_001278055.1:c.126A>C	NP_001264984.1:p.Arg42Ser
NM_014363.5:c.567A>C	NP_055178.3:p.Arg189Ser
XM_005266338.1:c.567A>C	XP_005266395.1:p.Arg189Ser
XM_011535038.1:c.591A>C	XP_011533340.1:p.Arg197Ser
XM_011535039.1:c.558A>C	XP_011533341.1:p.Arg186Ser
XM_005266338.2:c.567A>C	XP_005266395.1:p.Arg189Ser
XM_011535039.2:c.558A>C	XP_011533341.1:p.Arg186Ser
XM_017020539.1:c.558A>C	XP_016876028.1:p.Arg186Ser
XM_024449337.1:c.567A>C	XP_024305105.1:p.Arg189Ser
NM_014363.6:c.567A>C MANE Select	NP_055178.3:p.Arg189Ser
NM_001278055.2:c.126A>C	NP_001264984.1:p.Arg42Ser