Canonical Allele Identifier: CA387532958

Gene: SACS

Linked Data

• gnomAD v4: 13-23339858-A-C
• MyVariant Identifiers: chr13:g.23913997A>C (hg19) ; chr13:g.23339858A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23339858A>C , CM000675.2:g.23339858A>C	GRCh38
NC_000013.10:g.23913997A>C , CM000675.1:g.23913997A>C	GRCh37
NC_000013.9:g.22811997A>C	NCBI36
NG_012342.1:g.98845T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+13927T>G	ENSP00000508399.1:n.2185+13927T>G
ENST00000682944.1:c.4045T>G	ENSP00000507173.1:p.Tyr1349Asp
ENST00000683210.1:c.2185+13927T>G	ENSP00000506739.1:n.2185+13927T>G
ENST00000683270.1:c.4009T>G	ENSP00000507624.1:p.Tyr1337Asp
ENST00000683367.1:c.2177-10374T>G	ENSP00000507780.1:n.2177-10374T>G
ENST00000683489.1:c.2291+1727T>G	ENSP00000508403.1:n.2291+1727T>G
ENST00000683680.1:c.2318+1727T>G	ENSP00000507223.1:n.2318+1727T>G
ENST00000684163.1:c.2203+6953T>G	ENSP00000508262.1:n.2203+6953T>G
ENST00000684196.1:n.4543-10374T>G
ENST00000684325.1:c.2185+13927T>G	ENSP00000508121.1:n.2185+13927T>G
ENST00000684385.1:c.2220+6953T>G	ENSP00000507855.1:n.2220+6953T>G
ENST00000684497.1:c.2185+13927T>G	ENSP00000507057.1:n.2185+13927T>G
ENST00000382292.9:c.4018T>G MANE Select	ENSP00000371729.3:p.Tyr1340Asp
ENST00000423156.2:c.2186-10374T>G	ENSP00000390925.2:n.2186-10374T>G
ENST00000455470.6:c.2431+1587T>G	ENSP00000406565.2:n.2431+1587T>G
ENST00000382292.7:c.4018T>G	ENSP00000371729.3:p.Tyr1340Asp
ENST00000382298.7:c.4018T>G	ENSP00000371735.3:p.Tyr1340Asp
ENST00000402364.1:c.1768T>G	ENSP00000385844.1:p.Tyr590Asp
ENST00000423156.1:c.1058-10374T>G	ENSP00000390925.1:n.1058-10374T>G
ENST00000455470.5:c.2129+1587T>G
NM_001278055.1:c.3577T>G	NP_001264984.1:p.Tyr1193Asp
NM_014363.5:c.4018T>G	NP_055178.3:p.Tyr1340Asp
XM_005266338.1:c.4045T>G	XP_005266395.1:p.Tyr1349Asp
XM_011535038.1:c.4069T>G	XP_011533340.1:p.Tyr1357Asp
XM_011535039.1:c.4036T>G	XP_011533341.1:p.Tyr1346Asp
XM_005266338.2:c.4045T>G	XP_005266395.1:p.Tyr1349Asp
XM_011535039.2:c.4036T>G	XP_011533341.1:p.Tyr1346Asp
XM_017020539.1:c.4009T>G	XP_016876028.1:p.Tyr1337Asp
XM_024449337.1:c.4045T>G	XP_024305105.1:p.Tyr1349Asp
NM_014363.6:c.4018T>G MANE Select	NP_055178.3:p.Tyr1340Asp
NM_001278055.2:c.3577T>G	NP_001264984.1:p.Tyr1193Asp