Canonical Allele Identifier: CA387518813

Gene: SACS

Linked Data

• dbSNP Id: rs1868590781
• gnomAD v4: 13-23336336-A-G
• COSMIC: COSM2266173 ; COSM2266174
• MyVariant Identifiers: chr13:g.23910475A>G (hg19) ; chr13:g.23336336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336336A>G , CM000675.2:g.23336336A>G	GRCh38
NC_000013.10:g.23910475A>G , CM000675.1:g.23910475A>G	GRCh37
NC_000013.9:g.22808475A>G	NCBI36
NG_012342.1:g.102367T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17449T>C	ENSP00000508399.1:n.2185+17449T>C
ENST00000682944.1:c.7567T>C	ENSP00000507173.1:p.Cys2523Arg
ENST00000683210.1:c.2185+17449T>C	ENSP00000506739.1:n.2185+17449T>C
ENST00000683270.1:c.6445+1086T>C	ENSP00000507624.1:n.6445+1086T>C
ENST00000683367.1:c.2177-6852T>C	ENSP00000507780.1:n.2177-6852T>C
ENST00000683489.1:c.2291+5249T>C	ENSP00000508403.1:n.2291+5249T>C
ENST00000683680.1:c.2318+5249T>C	ENSP00000507223.1:n.2318+5249T>C
ENST00000684163.1:c.2204-6852T>C	ENSP00000508262.1:n.2204-6852T>C
ENST00000684196.1:n.4543-6852T>C
ENST00000684325.1:c.2186-14662T>C	ENSP00000508121.1:n.2186-14662T>C
ENST00000684385.1:c.2221-6852T>C	ENSP00000507855.1:n.2221-6852T>C
ENST00000684497.1:c.2186-13692T>C	ENSP00000507057.1:n.2186-13692T>C
ENST00000382292.9:c.7540T>C MANE Select	ENSP00000371729.3:p.Cys2514Arg
ENST00000423156.2:c.2186-6852T>C	ENSP00000390925.2:n.2186-6852T>C
ENST00000455470.6:c.2431+5109T>C	ENSP00000406565.2:n.2431+5109T>C
ENST00000382292.7:c.7540T>C	ENSP00000371729.3:p.Cys2514Arg
ENST00000382298.7:c.7540T>C	ENSP00000371735.3:p.Cys2514Arg
ENST00000402364.1:c.5290T>C	ENSP00000385844.1:p.Cys1764Arg
ENST00000423156.1:c.1058-6852T>C	ENSP00000390925.1:n.1058-6852T>C
ENST00000455470.5:c.2129+5109T>C
NM_001278055.1:c.7099T>C	NP_001264984.1:p.Cys2367Arg
NM_014363.5:c.7540T>C	NP_055178.3:p.Cys2514Arg
XM_005266338.1:c.7567T>C	XP_005266395.1:p.Cys2523Arg
XM_011535038.1:c.7591T>C	XP_011533340.1:p.Cys2531Arg
XM_011535039.1:c.7558T>C	XP_011533341.1:p.Cys2520Arg
XM_005266338.2:c.7567T>C	XP_005266395.1:p.Cys2523Arg
XM_011535039.2:c.7558T>C	XP_011533341.1:p.Cys2520Arg
XM_017020539.1:c.7531T>C	XP_016876028.1:p.Cys2511Arg
XM_024449337.1:c.7567T>C	XP_024305105.1:p.Cys2523Arg
NM_014363.6:c.7540T>C MANE Select	NP_055178.3:p.Cys2514Arg
NM_001278055.2:c.7099T>C	NP_001264984.1:p.Cys2367Arg