Canonical Allele Identifier: CA387521743

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911554G>A (hg19) ; chr13:g.23337415G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337415G>A , CM000675.2:g.23337415G>A	GRCh38
NC_000013.10:g.23911554G>A , CM000675.1:g.23911554G>A	GRCh37
NC_000013.9:g.22809554G>A	NCBI36
NG_012342.1:g.101288C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+16370C>T	ENSP00000508399.1:n.2185+16370C>T
ENST00000682944.1:c.6488C>T	ENSP00000507173.1:p.Ala2163Val
ENST00000683210.1:c.2185+16370C>T	ENSP00000506739.1:n.2185+16370C>T
ENST00000683270.1:c.6445+7C>T	ENSP00000507624.1:n.6445+7C>T
ENST00000683367.1:c.2177-7931C>T	ENSP00000507780.1:n.2177-7931C>T
ENST00000683489.1:c.2291+4170C>T	ENSP00000508403.1:n.2291+4170C>T
ENST00000683680.1:c.2318+4170C>T	ENSP00000507223.1:n.2318+4170C>T
ENST00000684163.1:c.2204-7931C>T	ENSP00000508262.1:n.2204-7931C>T
ENST00000684196.1:n.4543-7931C>T
ENST00000684325.1:c.2186-15741C>T	ENSP00000508121.1:n.2186-15741C>T
ENST00000684385.1:c.2221-7931C>T	ENSP00000507855.1:n.2221-7931C>T
ENST00000684497.1:c.2186-14771C>T	ENSP00000507057.1:n.2186-14771C>T
ENST00000382292.9:c.6461C>T MANE Select	ENSP00000371729.3:p.Ala2154Val
ENST00000423156.2:c.2186-7931C>T	ENSP00000390925.2:n.2186-7931C>T
ENST00000455470.6:c.2431+4030C>T	ENSP00000406565.2:n.2431+4030C>T
ENST00000382292.7:c.6461C>T	ENSP00000371729.3:p.Ala2154Val
ENST00000382298.7:c.6461C>T	ENSP00000371735.3:p.Ala2154Val
ENST00000402364.1:c.4211C>T	ENSP00000385844.1:p.Ala1404Val
ENST00000423156.1:c.1058-7931C>T	ENSP00000390925.1:n.1058-7931C>T
ENST00000455470.5:c.2129+4030C>T
NM_001278055.1:c.6020C>T	NP_001264984.1:p.Ala2007Val
NM_014363.5:c.6461C>T	NP_055178.3:p.Ala2154Val
XM_005266338.1:c.6488C>T	XP_005266395.1:p.Ala2163Val
XM_011535038.1:c.6512C>T	XP_011533340.1:p.Ala2171Val
XM_011535039.1:c.6479C>T	XP_011533341.1:p.Ala2160Val
XM_005266338.2:c.6488C>T	XP_005266395.1:p.Ala2163Val
XM_011535039.2:c.6479C>T	XP_011533341.1:p.Ala2160Val
XM_017020539.1:c.6452C>T	XP_016876028.1:p.Ala2151Val
XM_024449337.1:c.6488C>T	XP_024305105.1:p.Ala2163Val
NM_014363.6:c.6461C>T MANE Select	NP_055178.3:p.Ala2154Val
NM_001278055.2:c.6020C>T	NP_001264984.1:p.Ala2007Val