Canonical Allele Identifier: CA387510765

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23906929C>G (hg19) ; chr13:g.23332790C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23332790C>G , CM000675.2:g.23332790C>G	GRCh38
NC_000013.10:g.23906929C>G , CM000675.1:g.23906929C>G	GRCh37
NC_000013.9:g.22804929C>G	NCBI36
NG_012342.1:g.105913G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-20675G>C	ENSP00000508399.1:n.2186-20675G>C
ENST00000682944.1:c.11113G>C	ENSP00000507173.1:p.Val3705Leu
ENST00000683210.1:c.2185+20995G>C	ENSP00000506739.1:n.2185+20995G>C
ENST00000683270.1:c.6446-3306G>C	ENSP00000507624.1:n.6446-3306G>C
ENST00000683367.1:c.2177-3306G>C	ENSP00000507780.1:n.2177-3306G>C
ENST00000683489.1:c.2292-2838G>C	ENSP00000508403.1:n.2292-2838G>C
ENST00000683680.1:c.2319-2838G>C	ENSP00000507223.1:n.2319-2838G>C
ENST00000684163.1:c.2204-3306G>C	ENSP00000508262.1:n.2204-3306G>C
ENST00000684196.1:n.4543-3306G>C
ENST00000684325.1:c.2186-11116G>C	ENSP00000508121.1:n.2186-11116G>C
ENST00000684385.1:c.2221-3306G>C	ENSP00000507855.1:n.2221-3306G>C
ENST00000684497.1:c.2186-10146G>C	ENSP00000507057.1:n.2186-10146G>C
ENST00000382292.9:c.11086G>C MANE Select	ENSP00000371729.3:p.Val3696Leu
ENST00000423156.2:c.2186-3306G>C	ENSP00000390925.2:n.2186-3306G>C
ENST00000455470.6:c.2432-3306G>C	ENSP00000406565.2:n.2432-3306G>C
ENST00000382292.7:c.11086G>C	ENSP00000371729.3:p.Val3696Leu
ENST00000382298.7:c.11086G>C	ENSP00000371735.3:p.Val3696Leu
ENST00000402364.1:c.8836G>C	ENSP00000385844.1:p.Val2946Leu
ENST00000423156.1:c.1058-3306G>C	ENSP00000390925.1:n.1058-3306G>C
ENST00000455470.5:c.2130-3306G>C
NM_001278055.1:c.10645G>C	NP_001264984.1:p.Val3549Leu
NM_014363.5:c.11086G>C	NP_055178.3:p.Val3696Leu
XM_005266338.1:c.11113G>C	XP_005266395.1:p.Val3705Leu
XM_011535038.1:c.11137G>C	XP_011533340.1:p.Val3713Leu
XM_011535039.1:c.11104G>C	XP_011533341.1:p.Val3702Leu
XM_005266338.2:c.11113G>C	XP_005266395.1:p.Val3705Leu
XM_011535039.2:c.11104G>C	XP_011533341.1:p.Val3702Leu
XM_017020539.1:c.11077G>C	XP_016876028.1:p.Val3693Leu
XM_024449337.1:c.11113G>C	XP_024305105.1:p.Val3705Leu
NM_014363.6:c.11086G>C MANE Select	NP_055178.3:p.Val3696Leu
NM_001278055.2:c.10645G>C	NP_001264984.1:p.Val3549Leu