Canonical Allele Identifier: CA387525807

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23912638A>C (hg19) ; chr13:g.23338499A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23338499A>C , CM000675.2:g.23338499A>C	GRCh38
NC_000013.10:g.23912638A>C , CM000675.1:g.23912638A>C	GRCh37
NC_000013.9:g.22810638A>C	NCBI36
NG_012342.1:g.100204T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+15286T>G	ENSP00000508399.1:n.2185+15286T>G
ENST00000682944.1:c.5404T>G	ENSP00000507173.1:p.Phe1802Val
ENST00000683210.1:c.2185+15286T>G	ENSP00000506739.1:n.2185+15286T>G
ENST00000683270.1:c.5368T>G	ENSP00000507624.1:p.Phe1790Val
ENST00000683367.1:c.2177-9015T>G	ENSP00000507780.1:n.2177-9015T>G
ENST00000683489.1:c.2291+3086T>G	ENSP00000508403.1:n.2291+3086T>G
ENST00000683680.1:c.2318+3086T>G	ENSP00000507223.1:n.2318+3086T>G
ENST00000684163.1:c.2203+8312T>G	ENSP00000508262.1:n.2203+8312T>G
ENST00000684196.1:n.4543-9015T>G
ENST00000684325.1:c.2185+15286T>G	ENSP00000508121.1:n.2185+15286T>G
ENST00000684385.1:c.2220+8312T>G	ENSP00000507855.1:n.2220+8312T>G
ENST00000684497.1:c.2185+15286T>G	ENSP00000507057.1:n.2185+15286T>G
ENST00000382292.9:c.5377T>G MANE Select	ENSP00000371729.3:p.Phe1793Val
ENST00000423156.2:c.2186-9015T>G	ENSP00000390925.2:n.2186-9015T>G
ENST00000455470.6:c.2431+2946T>G	ENSP00000406565.2:n.2431+2946T>G
ENST00000382292.7:c.5377T>G	ENSP00000371729.3:p.Phe1793Val
ENST00000382298.7:c.5377T>G	ENSP00000371735.3:p.Phe1793Val
ENST00000402364.1:c.3127T>G	ENSP00000385844.1:p.Phe1043Val
ENST00000423156.1:c.1058-9015T>G	ENSP00000390925.1:n.1058-9015T>G
ENST00000455470.5:c.2129+2946T>G
NM_001278055.1:c.4936T>G	NP_001264984.1:p.Phe1646Val
NM_014363.5:c.5377T>G	NP_055178.3:p.Phe1793Val
XM_005266338.1:c.5404T>G	XP_005266395.1:p.Phe1802Val
XM_011535038.1:c.5428T>G	XP_011533340.1:p.Phe1810Val
XM_011535039.1:c.5395T>G	XP_011533341.1:p.Phe1799Val
XM_005266338.2:c.5404T>G	XP_005266395.1:p.Phe1802Val
XM_011535039.2:c.5395T>G	XP_011533341.1:p.Phe1799Val
XM_017020539.1:c.5368T>G	XP_016876028.1:p.Phe1790Val
XM_024449337.1:c.5404T>G	XP_024305105.1:p.Phe1802Val
NM_014363.6:c.5377T>G MANE Select	NP_055178.3:p.Phe1793Val
NM_001278055.2:c.4936T>G	NP_001264984.1:p.Phe1646Val