Canonical Allele Identifier: CA387511542

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907282A>T (hg19) ; chr13:g.23333143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333143A>T , CM000675.2:g.23333143A>T	GRCh38
NC_000013.10:g.23907282A>T , CM000675.1:g.23907282A>T	GRCh37
NC_000013.9:g.22805282A>T	NCBI36
NG_012342.1:g.105560T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+20642T>A	ENSP00000508399.1:n.2185+20642T>A
ENST00000682944.1:c.10760T>A	ENSP00000507173.1:p.Phe3587Tyr
ENST00000683210.1:c.2185+20642T>A	ENSP00000506739.1:n.2185+20642T>A
ENST00000683270.1:c.6446-3659T>A	ENSP00000507624.1:n.6446-3659T>A
ENST00000683367.1:c.2177-3659T>A	ENSP00000507780.1:n.2177-3659T>A
ENST00000683489.1:c.2292-3191T>A	ENSP00000508403.1:n.2292-3191T>A
ENST00000683680.1:c.2319-3191T>A	ENSP00000507223.1:n.2319-3191T>A
ENST00000684163.1:c.2204-3659T>A	ENSP00000508262.1:n.2204-3659T>A
ENST00000684196.1:n.4543-3659T>A
ENST00000684325.1:c.2186-11469T>A	ENSP00000508121.1:n.2186-11469T>A
ENST00000684385.1:c.2221-3659T>A	ENSP00000507855.1:n.2221-3659T>A
ENST00000684497.1:c.2186-10499T>A	ENSP00000507057.1:n.2186-10499T>A
ENST00000382292.9:c.10733T>A MANE Select	ENSP00000371729.3:p.Phe3578Tyr
ENST00000423156.2:c.2186-3659T>A	ENSP00000390925.2:n.2186-3659T>A
ENST00000455470.6:c.2432-3659T>A	ENSP00000406565.2:n.2432-3659T>A
ENST00000382292.7:c.10733T>A	ENSP00000371729.3:p.Phe3578Tyr
ENST00000382298.7:c.10733T>A	ENSP00000371735.3:p.Phe3578Tyr
ENST00000402364.1:c.8483T>A	ENSP00000385844.1:p.Phe2828Tyr
ENST00000423156.1:c.1058-3659T>A	ENSP00000390925.1:n.1058-3659T>A
ENST00000455470.5:c.2130-3659T>A
NM_001278055.1:c.10292T>A	NP_001264984.1:p.Phe3431Tyr
NM_014363.5:c.10733T>A	NP_055178.3:p.Phe3578Tyr
XM_005266338.1:c.10760T>A	XP_005266395.1:p.Phe3587Tyr
XM_011535038.1:c.10784T>A	XP_011533340.1:p.Phe3595Tyr
XM_011535039.1:c.10751T>A	XP_011533341.1:p.Phe3584Tyr
XM_005266338.2:c.10760T>A	XP_005266395.1:p.Phe3587Tyr
XM_011535039.2:c.10751T>A	XP_011533341.1:p.Phe3584Tyr
XM_017020539.1:c.10724T>A	XP_016876028.1:p.Phe3575Tyr
XM_024449337.1:c.10760T>A	XP_024305105.1:p.Phe3587Tyr
NM_014363.6:c.10733T>A MANE Select	NP_055178.3:p.Phe3578Tyr
NM_001278055.2:c.10292T>A	NP_001264984.1:p.Phe3431Tyr