Canonical Allele Identifier: CA387540603

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23915811A>C (hg19) ; chr13:g.23341672A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341672A>C , CM000675.2:g.23341672A>C	GRCh38
NC_000013.10:g.23915811A>C , CM000675.1:g.23915811A>C	GRCh37
NC_000013.9:g.22813811A>C	NCBI36
NG_012342.1:g.97031T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12113T>G	ENSP00000508399.1:n.2185+12113T>G
ENST00000682944.1:c.2231T>G	ENSP00000507173.1:p.Leu744Arg
ENST00000683210.1:c.2185+12113T>G	ENSP00000506739.1:n.2185+12113T>G
ENST00000683270.1:c.2195T>G	ENSP00000507624.1:p.Leu732Arg
ENST00000683367.1:c.2176+12113T>G	ENSP00000507780.1:n.2176+12113T>G
ENST00000683489.1:c.2204T>G	ENSP00000508403.1:p.Leu735Arg
ENST00000683680.1:c.2231T>G	ENSP00000507223.1:p.Leu744Arg
ENST00000684163.1:c.2203+5139T>G	ENSP00000508262.1:n.2203+5139T>G
ENST00000684196.1:n.4542+12113T>G
ENST00000684325.1:c.2185+12113T>G	ENSP00000508121.1:n.2185+12113T>G
ENST00000684385.1:c.2220+5139T>G	ENSP00000507855.1:n.2220+5139T>G
ENST00000684497.1:c.2185+12113T>G	ENSP00000507057.1:n.2185+12113T>G
ENST00000382292.9:c.2204T>G MANE Select	ENSP00000371729.3:p.Leu735Arg
ENST00000423156.2:c.2185+12113T>G	ENSP00000390925.2:n.2185+12113T>G
ENST00000455470.6:c.2204T>G	ENSP00000406565.2:p.Leu735Arg
ENST00000382292.7:c.2204T>G	ENSP00000371729.3:p.Leu735Arg
ENST00000382298.7:c.2204T>G	ENSP00000371735.3:p.Leu735Arg
ENST00000402364.1:c.-47T>G	ENSP00000385844.1:n.-47T>G
ENST00000423156.1:c.1057+12113T>G	ENSP00000390925.1:n.1057+12113T>G
ENST00000455470.5:c.1902T>G
NM_001278055.1:c.1763T>G	NP_001264984.1:p.Leu588Arg
NM_014363.5:c.2204T>G	NP_055178.3:p.Leu735Arg
XM_005266338.1:c.2231T>G	XP_005266395.1:p.Leu744Arg
XM_011535038.1:c.2255T>G	XP_011533340.1:p.Leu752Arg
XM_011535039.1:c.2222T>G	XP_011533341.1:p.Leu741Arg
XM_005266338.2:c.2231T>G	XP_005266395.1:p.Leu744Arg
XM_011535039.2:c.2222T>G	XP_011533341.1:p.Leu741Arg
XM_017020539.1:c.2195T>G	XP_016876028.1:p.Leu732Arg
XM_024449337.1:c.2231T>G	XP_024305105.1:p.Leu744Arg
NM_014363.6:c.2204T>G MANE Select	NP_055178.3:p.Leu735Arg
NM_001278055.2:c.1763T>G	NP_001264984.1:p.Leu588Arg