Canonical Allele Identifier: CA387540572

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23915796G>T (hg19) ; chr13:g.23341657G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341657G>T , CM000675.2:g.23341657G>T	GRCh38
NC_000013.10:g.23915796G>T , CM000675.1:g.23915796G>T	GRCh37
NC_000013.9:g.22813796G>T	NCBI36
NG_012342.1:g.97046C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+12128C>A	ENSP00000508399.1:n.2185+12128C>A
ENST00000682944.1:c.2246C>A	ENSP00000507173.1:p.Pro749Gln
ENST00000683210.1:c.2185+12128C>A	ENSP00000506739.1:n.2185+12128C>A
ENST00000683270.1:c.2210C>A	ENSP00000507624.1:p.Pro737Gln
ENST00000683367.1:c.2176+12128C>A	ENSP00000507780.1:n.2176+12128C>A
ENST00000683489.1:c.2219C>A	ENSP00000508403.1:p.Pro740Gln
ENST00000683680.1:c.2246C>A	ENSP00000507223.1:p.Pro749Gln
ENST00000684163.1:c.2203+5154C>A	ENSP00000508262.1:n.2203+5154C>A
ENST00000684196.1:n.4542+12128C>A
ENST00000684325.1:c.2185+12128C>A	ENSP00000508121.1:n.2185+12128C>A
ENST00000684385.1:c.2220+5154C>A	ENSP00000507855.1:n.2220+5154C>A
ENST00000684497.1:c.2185+12128C>A	ENSP00000507057.1:n.2185+12128C>A
ENST00000382292.9:c.2219C>A MANE Select	ENSP00000371729.3:p.Pro740Gln
ENST00000423156.2:c.2185+12128C>A	ENSP00000390925.2:n.2185+12128C>A
ENST00000455470.6:c.2219C>A	ENSP00000406565.2:p.Pro740Gln
ENST00000382292.7:c.2219C>A	ENSP00000371729.3:p.Pro740Gln
ENST00000382298.7:c.2219C>A	ENSP00000371735.3:p.Pro740Gln
ENST00000402364.1:c.-32C>A	ENSP00000385844.1:n.-32C>A
ENST00000423156.1:c.1057+12128C>A	ENSP00000390925.1:n.1057+12128C>A
ENST00000455470.5:c.1917C>A
NM_001278055.1:c.1778C>A	NP_001264984.1:p.Pro593Gln
NM_014363.5:c.2219C>A	NP_055178.3:p.Pro740Gln
XM_005266338.1:c.2246C>A	XP_005266395.1:p.Pro749Gln
XM_011535038.1:c.2270C>A	XP_011533340.1:p.Pro757Gln
XM_011535039.1:c.2237C>A	XP_011533341.1:p.Pro746Gln
XM_005266338.2:c.2246C>A	XP_005266395.1:p.Pro749Gln
XM_011535039.2:c.2237C>A	XP_011533341.1:p.Pro746Gln
XM_017020539.1:c.2210C>A	XP_016876028.1:p.Pro737Gln
XM_024449337.1:c.2246C>A	XP_024305105.1:p.Pro749Gln
NM_014363.6:c.2219C>A MANE Select	NP_055178.3:p.Pro740Gln
NM_001278055.2:c.1778C>A	NP_001264984.1:p.Pro593Gln