Canonical Allele Identifier: CA387513189

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23908015A>C (hg19) ; chr13:g.23333876A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333876A>C , CM000675.2:g.23333876A>C	GRCh38
NC_000013.10:g.23908015A>C , CM000675.1:g.23908015A>C	GRCh37
NC_000013.9:g.22806015A>C	NCBI36
NG_012342.1:g.104827T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+19909T>G	ENSP00000508399.1:n.2185+19909T>G
ENST00000682944.1:c.10027T>G	ENSP00000507173.1:p.Leu3343Val
ENST00000683210.1:c.2185+19909T>G	ENSP00000506739.1:n.2185+19909T>G
ENST00000683270.1:c.6445+3546T>G	ENSP00000507624.1:n.6445+3546T>G
ENST00000683367.1:c.2177-4392T>G	ENSP00000507780.1:n.2177-4392T>G
ENST00000683489.1:c.2292-3924T>G	ENSP00000508403.1:n.2292-3924T>G
ENST00000683680.1:c.2319-3924T>G	ENSP00000507223.1:n.2319-3924T>G
ENST00000684163.1:c.2204-4392T>G	ENSP00000508262.1:n.2204-4392T>G
ENST00000684196.1:n.4543-4392T>G
ENST00000684325.1:c.2186-12202T>G	ENSP00000508121.1:n.2186-12202T>G
ENST00000684385.1:c.2221-4392T>G	ENSP00000507855.1:n.2221-4392T>G
ENST00000684497.1:c.2186-11232T>G	ENSP00000507057.1:n.2186-11232T>G
ENST00000382292.9:c.10000T>G MANE Select	ENSP00000371729.3:p.Leu3334Val
ENST00000423156.2:c.2186-4392T>G	ENSP00000390925.2:n.2186-4392T>G
ENST00000455470.6:c.2432-4392T>G	ENSP00000406565.2:n.2432-4392T>G
ENST00000382292.7:c.10000T>G	ENSP00000371729.3:p.Leu3334Val
ENST00000382298.7:c.10000T>G	ENSP00000371735.3:p.Leu3334Val
ENST00000402364.1:c.7750T>G	ENSP00000385844.1:p.Leu2584Val
ENST00000423156.1:c.1058-4392T>G	ENSP00000390925.1:n.1058-4392T>G
ENST00000455470.5:c.2130-4392T>G
NM_001278055.1:c.9559T>G	NP_001264984.1:p.Leu3187Val
NM_014363.5:c.10000T>G	NP_055178.3:p.Leu3334Val
XM_005266338.1:c.10027T>G	XP_005266395.1:p.Leu3343Val
XM_011535038.1:c.10051T>G	XP_011533340.1:p.Leu3351Val
XM_011535039.1:c.10018T>G	XP_011533341.1:p.Leu3340Val
XM_005266338.2:c.10027T>G	XP_005266395.1:p.Leu3343Val
XM_011535039.2:c.10018T>G	XP_011533341.1:p.Leu3340Val
XM_017020539.1:c.9991T>G	XP_016876028.1:p.Leu3331Val
XM_024449337.1:c.10027T>G	XP_024305105.1:p.Leu3343Val
NM_014363.6:c.10000T>G MANE Select	NP_055178.3:p.Leu3334Val
NM_001278055.2:c.9559T>G	NP_001264984.1:p.Leu3187Val