Canonical Allele Identifier: CA387516706

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909609T>C (hg19) ; chr13:g.23335470T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23335470T>C , CM000675.2:g.23335470T>C	GRCh38
NC_000013.10:g.23909609T>C , CM000675.1:g.23909609T>C	GRCh37
NC_000013.9:g.22807609T>C	NCBI36
NG_012342.1:g.103233A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18315A>G	ENSP00000508399.1:n.2185+18315A>G
ENST00000682944.1:c.8433A>G	ENSP00000507173.1:p.Ile2811Met
ENST00000683210.1:c.2185+18315A>G	ENSP00000506739.1:n.2185+18315A>G
ENST00000683270.1:c.6445+1952A>G	ENSP00000507624.1:n.6445+1952A>G
ENST00000683367.1:c.2177-5986A>G	ENSP00000507780.1:n.2177-5986A>G
ENST00000683489.1:c.2292-5518A>G	ENSP00000508403.1:n.2292-5518A>G
ENST00000683680.1:c.2319-5518A>G	ENSP00000507223.1:n.2319-5518A>G
ENST00000684163.1:c.2204-5986A>G	ENSP00000508262.1:n.2204-5986A>G
ENST00000684196.1:n.4543-5986A>G
ENST00000684325.1:c.2186-13796A>G	ENSP00000508121.1:n.2186-13796A>G
ENST00000684385.1:c.2221-5986A>G	ENSP00000507855.1:n.2221-5986A>G
ENST00000684497.1:c.2186-12826A>G	ENSP00000507057.1:n.2186-12826A>G
ENST00000382292.9:c.8406A>G MANE Select	ENSP00000371729.3:p.Ile2802Met
ENST00000423156.2:c.2186-5986A>G	ENSP00000390925.2:n.2186-5986A>G
ENST00000455470.6:c.2431+5975A>G	ENSP00000406565.2:n.2431+5975A>G
ENST00000382292.7:c.8406A>G	ENSP00000371729.3:p.Ile2802Met
ENST00000382298.7:c.8406A>G	ENSP00000371735.3:p.Ile2802Met
ENST00000402364.1:c.6156A>G	ENSP00000385844.1:p.Ile2052Met
ENST00000423156.1:c.1058-5986A>G	ENSP00000390925.1:n.1058-5986A>G
ENST00000455470.5:c.2129+5975A>G
NM_001278055.1:c.7965A>G	NP_001264984.1:p.Ile2655Met
NM_014363.5:c.8406A>G	NP_055178.3:p.Ile2802Met
XM_005266338.1:c.8433A>G	XP_005266395.1:p.Ile2811Met
XM_011535038.1:c.8457A>G	XP_011533340.1:p.Ile2819Met
XM_011535039.1:c.8424A>G	XP_011533341.1:p.Ile2808Met
XM_005266338.2:c.8433A>G	XP_005266395.1:p.Ile2811Met
XM_011535039.2:c.8424A>G	XP_011533341.1:p.Ile2808Met
XM_017020539.1:c.8397A>G	XP_016876028.1:p.Ile2799Met
XM_024449337.1:c.8433A>G	XP_024305105.1:p.Ile2811Met
NM_014363.6:c.8406A>G MANE Select	NP_055178.3:p.Ile2802Met
NM_001278055.2:c.7965A>G	NP_001264984.1:p.Ile2655Met