Canonical Allele Identifier: CA387512166

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907555T>G (hg19) ; chr13:g.23333416T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333416T>G , CM000675.2:g.23333416T>G	GRCh38
NC_000013.10:g.23907555T>G , CM000675.1:g.23907555T>G	GRCh37
NC_000013.9:g.22805555T>G	NCBI36
NG_012342.1:g.105287A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20369A>C	ENSP00000508399.1:n.2185+20369A>C
ENST00000682944.1:c.10487A>C	ENSP00000507173.1:p.Asn3496Thr
ENST00000683210.1:c.2185+20369A>C	ENSP00000506739.1:n.2185+20369A>C
ENST00000683270.1:c.6446-3932A>C	ENSP00000507624.1:n.6446-3932A>C
ENST00000683367.1:c.2177-3932A>C	ENSP00000507780.1:n.2177-3932A>C
ENST00000683489.1:c.2292-3464A>C	ENSP00000508403.1:n.2292-3464A>C
ENST00000683680.1:c.2319-3464A>C	ENSP00000507223.1:n.2319-3464A>C
ENST00000684163.1:c.2204-3932A>C	ENSP00000508262.1:n.2204-3932A>C
ENST00000684196.1:n.4543-3932A>C
ENST00000684325.1:c.2186-11742A>C	ENSP00000508121.1:n.2186-11742A>C
ENST00000684385.1:c.2221-3932A>C	ENSP00000507855.1:n.2221-3932A>C
ENST00000684497.1:c.2186-10772A>C	ENSP00000507057.1:n.2186-10772A>C
ENST00000382292.9:c.10460A>C MANE Select	ENSP00000371729.3:p.Asn3487Thr
ENST00000423156.2:c.2186-3932A>C	ENSP00000390925.2:n.2186-3932A>C
ENST00000455470.6:c.2432-3932A>C	ENSP00000406565.2:n.2432-3932A>C
ENST00000382292.7:c.10460A>C	ENSP00000371729.3:p.Asn3487Thr
ENST00000382298.7:c.10460A>C	ENSP00000371735.3:p.Asn3487Thr
ENST00000402364.1:c.8210A>C	ENSP00000385844.1:p.Asn2737Thr
ENST00000423156.1:c.1058-3932A>C	ENSP00000390925.1:n.1058-3932A>C
ENST00000455470.5:c.2130-3932A>C
NM_001278055.1:c.10019A>C	NP_001264984.1:p.Asn3340Thr
NM_014363.5:c.10460A>C	NP_055178.3:p.Asn3487Thr
XM_005266338.1:c.10487A>C	XP_005266395.1:p.Asn3496Thr
XM_011535038.1:c.10511A>C	XP_011533340.1:p.Asn3504Thr
XM_011535039.1:c.10478A>C	XP_011533341.1:p.Asn3493Thr
XM_005266338.2:c.10487A>C	XP_005266395.1:p.Asn3496Thr
XM_011535039.2:c.10478A>C	XP_011533341.1:p.Asn3493Thr
XM_017020539.1:c.10451A>C	XP_016876028.1:p.Asn3484Thr
XM_024449337.1:c.10487A>C	XP_024305105.1:p.Asn3496Thr
NM_014363.6:c.10460A>C MANE Select	NP_055178.3:p.Asn3487Thr
NM_001278055.2:c.10019A>C	NP_001264984.1:p.Asn3340Thr