Canonical Allele Identifier: CA387523382

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911680C>G (hg19) ; chr13:g.23337541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337541C>G , CM000675.2:g.23337541C>G	GRCh38
NC_000013.10:g.23911680C>G , CM000675.1:g.23911680C>G	GRCh37
NC_000013.9:g.22809680C>G	NCBI36
NG_012342.1:g.101162G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16244G>C	ENSP00000508399.1:n.2185+16244G>C
ENST00000682944.1:c.6362G>C	ENSP00000507173.1:p.Arg2121Thr
ENST00000683210.1:c.2185+16244G>C	ENSP00000506739.1:n.2185+16244G>C
ENST00000683270.1:c.6326G>C	ENSP00000507624.1:p.Arg2109Thr
ENST00000683367.1:c.2177-8057G>C	ENSP00000507780.1:n.2177-8057G>C
ENST00000683489.1:c.2291+4044G>C	ENSP00000508403.1:n.2291+4044G>C
ENST00000683680.1:c.2318+4044G>C	ENSP00000507223.1:n.2318+4044G>C
ENST00000684163.1:c.2204-8057G>C	ENSP00000508262.1:n.2204-8057G>C
ENST00000684196.1:n.4543-8057G>C
ENST00000684325.1:c.2186-15867G>C	ENSP00000508121.1:n.2186-15867G>C
ENST00000684385.1:c.2221-8057G>C	ENSP00000507855.1:n.2221-8057G>C
ENST00000684497.1:c.2186-14897G>C	ENSP00000507057.1:n.2186-14897G>C
ENST00000382292.9:c.6335G>C MANE Select	ENSP00000371729.3:p.Arg2112Thr
ENST00000423156.2:c.2186-8057G>C	ENSP00000390925.2:n.2186-8057G>C
ENST00000455470.6:c.2431+3904G>C	ENSP00000406565.2:n.2431+3904G>C
ENST00000382292.7:c.6335G>C	ENSP00000371729.3:p.Arg2112Thr
ENST00000382298.7:c.6335G>C	ENSP00000371735.3:p.Arg2112Thr
ENST00000402364.1:c.4085G>C	ENSP00000385844.1:p.Arg1362Thr
ENST00000423156.1:c.1058-8057G>C	ENSP00000390925.1:n.1058-8057G>C
ENST00000455470.5:c.2129+3904G>C
NM_001278055.1:c.5894G>C	NP_001264984.1:p.Arg1965Thr
NM_014363.5:c.6335G>C	NP_055178.3:p.Arg2112Thr
XM_005266338.1:c.6362G>C	XP_005266395.1:p.Arg2121Thr
XM_011535038.1:c.6386G>C	XP_011533340.1:p.Arg2129Thr
XM_011535039.1:c.6353G>C	XP_011533341.1:p.Arg2118Thr
XM_005266338.2:c.6362G>C	XP_005266395.1:p.Arg2121Thr
XM_011535039.2:c.6353G>C	XP_011533341.1:p.Arg2118Thr
XM_017020539.1:c.6326G>C	XP_016876028.1:p.Arg2109Thr
XM_024449337.1:c.6362G>C	XP_024305105.1:p.Arg2121Thr
NM_014363.6:c.6335G>C MANE Select	NP_055178.3:p.Arg2112Thr
NM_001278055.2:c.5894G>C	NP_001264984.1:p.Arg1965Thr