Canonical Allele Identifier: CA387506772

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23905156T>G (hg19) ; chr13:g.23331017T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23331017T>G , CM000675.2:g.23331017T>G	GRCh38
NC_000013.10:g.23905156T>G , CM000675.1:g.23905156T>G	GRCh37
NC_000013.9:g.22803156T>G	NCBI36
NG_012342.1:g.107686A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18902A>C	ENSP00000508399.1:n.2186-18902A>C
ENST00000682944.1:c.12886A>C	ENSP00000507173.1:p.Lys4296Gln
ENST00000683210.1:c.2185+22768A>C	ENSP00000506739.1:n.2185+22768A>C
ENST00000683270.1:c.6446-1533A>C	ENSP00000507624.1:n.6446-1533A>C
ENST00000683367.1:c.2177-1533A>C	ENSP00000507780.1:n.2177-1533A>C
ENST00000683489.1:c.2292-1065A>C	ENSP00000508403.1:n.2292-1065A>C
ENST00000683680.1:c.2319-1065A>C	ENSP00000507223.1:n.2319-1065A>C
ENST00000684163.1:c.2204-1533A>C	ENSP00000508262.1:n.2204-1533A>C
ENST00000684196.1:n.4543-1533A>C
ENST00000684325.1:c.2186-9343A>C	ENSP00000508121.1:n.2186-9343A>C
ENST00000684385.1:c.2221-1533A>C	ENSP00000507855.1:n.2221-1533A>C
ENST00000684497.1:c.2186-8373A>C	ENSP00000507057.1:n.2186-8373A>C
ENST00000382292.9:c.12859A>C MANE Select	ENSP00000371729.3:p.Lys4287Gln
ENST00000423156.2:c.2186-1533A>C	ENSP00000390925.2:n.2186-1533A>C
ENST00000455470.6:c.2432-1533A>C	ENSP00000406565.2:n.2432-1533A>C
ENST00000382292.7:c.12859A>C	ENSP00000371729.3:p.Lys4287Gln
ENST00000382298.7:c.12859A>C	ENSP00000371735.3:p.Lys4287Gln
ENST00000402364.1:c.10609A>C	ENSP00000385844.1:p.Lys3537Gln
ENST00000423156.1:c.1058-1533A>C	ENSP00000390925.1:n.1058-1533A>C
ENST00000455470.5:c.2130-1533A>C
NM_001278055.1:c.12418A>C	NP_001264984.1:p.Lys4140Gln
NM_014363.5:c.12859A>C	NP_055178.3:p.Lys4287Gln
XM_005266338.1:c.12886A>C	XP_005266395.1:p.Lys4296Gln
XM_011535038.1:c.12910A>C	XP_011533340.1:p.Lys4304Gln
XM_011535039.1:c.12877A>C	XP_011533341.1:p.Lys4293Gln
XM_005266338.2:c.12886A>C	XP_005266395.1:p.Lys4296Gln
XM_011535039.2:c.12877A>C	XP_011533341.1:p.Lys4293Gln
XM_017020539.1:c.12850A>C	XP_016876028.1:p.Lys4284Gln
XM_024449337.1:c.12886A>C	XP_024305105.1:p.Lys4296Gln
NM_014363.6:c.12859A>C MANE Select	NP_055178.3:p.Lys4287Gln
NM_001278055.2:c.12418A>C	NP_001264984.1:p.Lys4140Gln