Canonical Allele Identifier: CA387539069

Gene: SACS

Linked Data

• gnomAD v4: 13-23341456-A-G
• MyVariant Identifiers: chr13:g.23915595A>G (hg19) ; chr13:g.23341456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341456A>G , CM000675.2:g.23341456A>G	GRCh38
NC_000013.10:g.23915595A>G , CM000675.1:g.23915595A>G	GRCh37
NC_000013.9:g.22813595A>G	NCBI36
NG_012342.1:g.97247T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+12329T>C	ENSP00000508399.1:n.2185+12329T>C
ENST00000682944.1:c.2447T>C	ENSP00000507173.1:p.Ile816Thr
ENST00000683210.1:c.2185+12329T>C	ENSP00000506739.1:n.2185+12329T>C
ENST00000683270.1:c.2411T>C	ENSP00000507624.1:p.Ile804Thr
ENST00000683367.1:c.2177-11972T>C	ENSP00000507780.1:n.2177-11972T>C
ENST00000683489.1:c.2291+129T>C	ENSP00000508403.1:n.2291+129T>C
ENST00000683680.1:c.2318+129T>C	ENSP00000507223.1:n.2318+129T>C
ENST00000684163.1:c.2203+5355T>C	ENSP00000508262.1:n.2203+5355T>C
ENST00000684196.1:n.4543-11972T>C
ENST00000684325.1:c.2185+12329T>C	ENSP00000508121.1:n.2185+12329T>C
ENST00000684385.1:c.2220+5355T>C	ENSP00000507855.1:n.2220+5355T>C
ENST00000684497.1:c.2185+12329T>C	ENSP00000507057.1:n.2185+12329T>C
ENST00000382292.9:c.2420T>C MANE Select	ENSP00000371729.3:p.Ile807Thr
ENST00000423156.2:c.2186-11972T>C	ENSP00000390925.2:n.2186-11972T>C
ENST00000455470.6:c.2420T>C	ENSP00000406565.2:p.Ile807Thr
ENST00000382292.7:c.2420T>C	ENSP00000371729.3:p.Ile807Thr
ENST00000382298.7:c.2420T>C	ENSP00000371735.3:p.Ile807Thr
ENST00000402364.1:c.170T>C	ENSP00000385844.1:p.Ile57Thr
ENST00000423156.1:c.1058-11972T>C	ENSP00000390925.1:n.1058-11972T>C
ENST00000455470.5:c.2118T>C
NM_001278055.1:c.1979T>C	NP_001264984.1:p.Ile660Thr
NM_014363.5:c.2420T>C	NP_055178.3:p.Ile807Thr
XM_005266338.1:c.2447T>C	XP_005266395.1:p.Ile816Thr
XM_011535038.1:c.2471T>C	XP_011533340.1:p.Ile824Thr
XM_011535039.1:c.2438T>C	XP_011533341.1:p.Ile813Thr
XM_005266338.2:c.2447T>C	XP_005266395.1:p.Ile816Thr
XM_011535039.2:c.2438T>C	XP_011533341.1:p.Ile813Thr
XM_017020539.1:c.2411T>C	XP_016876028.1:p.Ile804Thr
XM_024449337.1:c.2447T>C	XP_024305105.1:p.Ile816Thr
NM_014363.6:c.2420T>C MANE Select	NP_055178.3:p.Ile807Thr
NM_001278055.2:c.1979T>C	NP_001264984.1:p.Ile660Thr