Canonical Allele Identifier: CA387513122

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907988C>A (hg19) ; chr13:g.23333849C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333849C>A , CM000675.2:g.23333849C>A	GRCh38
NC_000013.10:g.23907988C>A , CM000675.1:g.23907988C>A	GRCh37
NC_000013.9:g.22805988C>A	NCBI36
NG_012342.1:g.104854G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+19936G>T	ENSP00000508399.1:n.2185+19936G>T
ENST00000682944.1:c.10054G>T	ENSP00000507173.1:p.Ala3352Ser
ENST00000683210.1:c.2185+19936G>T	ENSP00000506739.1:n.2185+19936G>T
ENST00000683270.1:c.6445+3573G>T	ENSP00000507624.1:n.6445+3573G>T
ENST00000683367.1:c.2177-4365G>T	ENSP00000507780.1:n.2177-4365G>T
ENST00000683489.1:c.2292-3897G>T	ENSP00000508403.1:n.2292-3897G>T
ENST00000683680.1:c.2319-3897G>T	ENSP00000507223.1:n.2319-3897G>T
ENST00000684163.1:c.2204-4365G>T	ENSP00000508262.1:n.2204-4365G>T
ENST00000684196.1:n.4543-4365G>T
ENST00000684325.1:c.2186-12175G>T	ENSP00000508121.1:n.2186-12175G>T
ENST00000684385.1:c.2221-4365G>T	ENSP00000507855.1:n.2221-4365G>T
ENST00000684497.1:c.2186-11205G>T	ENSP00000507057.1:n.2186-11205G>T
ENST00000382292.9:c.10027G>T MANE Select	ENSP00000371729.3:p.Ala3343Ser
ENST00000423156.2:c.2186-4365G>T	ENSP00000390925.2:n.2186-4365G>T
ENST00000455470.6:c.2432-4365G>T	ENSP00000406565.2:n.2432-4365G>T
ENST00000382292.7:c.10027G>T	ENSP00000371729.3:p.Ala3343Ser
ENST00000382298.7:c.10027G>T	ENSP00000371735.3:p.Ala3343Ser
ENST00000402364.1:c.7777G>T	ENSP00000385844.1:p.Ala2593Ser
ENST00000423156.1:c.1058-4365G>T	ENSP00000390925.1:n.1058-4365G>T
ENST00000455470.5:c.2130-4365G>T
NM_001278055.1:c.9586G>T	NP_001264984.1:p.Ala3196Ser
NM_014363.5:c.10027G>T	NP_055178.3:p.Ala3343Ser
XM_005266338.1:c.10054G>T	XP_005266395.1:p.Ala3352Ser
XM_011535038.1:c.10078G>T	XP_011533340.1:p.Ala3360Ser
XM_011535039.1:c.10045G>T	XP_011533341.1:p.Ala3349Ser
XM_005266338.2:c.10054G>T	XP_005266395.1:p.Ala3352Ser
XM_011535039.2:c.10045G>T	XP_011533341.1:p.Ala3349Ser
XM_017020539.1:c.10018G>T	XP_016876028.1:p.Ala3340Ser
XM_024449337.1:c.10054G>T	XP_024305105.1:p.Ala3352Ser
NM_014363.6:c.10027G>T MANE Select	NP_055178.3:p.Ala3343Ser
NM_001278055.2:c.9586G>T	NP_001264984.1:p.Ala3196Ser