Canonical Allele Identifier: CA387514951

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23908809A>G (hg19) ; chr13:g.23334670A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334670A>G , CM000675.2:g.23334670A>G	GRCh38
NC_000013.10:g.23908809A>G , CM000675.1:g.23908809A>G	GRCh37
NC_000013.9:g.22806809A>G	NCBI36
NG_012342.1:g.104033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19115T>C	ENSP00000508399.1:n.2185+19115T>C
ENST00000682944.1:c.9233T>C	ENSP00000507173.1:p.Leu3078Ser
ENST00000683210.1:c.2185+19115T>C	ENSP00000506739.1:n.2185+19115T>C
ENST00000683270.1:c.6445+2752T>C	ENSP00000507624.1:n.6445+2752T>C
ENST00000683367.1:c.2177-5186T>C	ENSP00000507780.1:n.2177-5186T>C
ENST00000683489.1:c.2292-4718T>C	ENSP00000508403.1:n.2292-4718T>C
ENST00000683680.1:c.2319-4718T>C	ENSP00000507223.1:n.2319-4718T>C
ENST00000684163.1:c.2204-5186T>C	ENSP00000508262.1:n.2204-5186T>C
ENST00000684196.1:n.4543-5186T>C
ENST00000684325.1:c.2186-12996T>C	ENSP00000508121.1:n.2186-12996T>C
ENST00000684385.1:c.2221-5186T>C	ENSP00000507855.1:n.2221-5186T>C
ENST00000684497.1:c.2186-12026T>C	ENSP00000507057.1:n.2186-12026T>C
ENST00000382292.9:c.9206T>C MANE Select	ENSP00000371729.3:p.Leu3069Ser
ENST00000423156.2:c.2186-5186T>C	ENSP00000390925.2:n.2186-5186T>C
ENST00000455470.6:c.2432-5186T>C	ENSP00000406565.2:n.2432-5186T>C
ENST00000382292.7:c.9206T>C	ENSP00000371729.3:p.Leu3069Ser
ENST00000382298.7:c.9206T>C	ENSP00000371735.3:p.Leu3069Ser
ENST00000402364.1:c.6956T>C	ENSP00000385844.1:p.Leu2319Ser
ENST00000423156.1:c.1058-5186T>C	ENSP00000390925.1:n.1058-5186T>C
ENST00000455470.5:c.2130-5186T>C
NM_001278055.1:c.8765T>C	NP_001264984.1:p.Leu2922Ser
NM_014363.5:c.9206T>C	NP_055178.3:p.Leu3069Ser
XM_005266338.1:c.9233T>C	XP_005266395.1:p.Leu3078Ser
XM_011535038.1:c.9257T>C	XP_011533340.1:p.Leu3086Ser
XM_011535039.1:c.9224T>C	XP_011533341.1:p.Leu3075Ser
XM_005266338.2:c.9233T>C	XP_005266395.1:p.Leu3078Ser
XM_011535039.2:c.9224T>C	XP_011533341.1:p.Leu3075Ser
XM_017020539.1:c.9197T>C	XP_016876028.1:p.Leu3066Ser
XM_024449337.1:c.9233T>C	XP_024305105.1:p.Leu3078Ser
NM_014363.6:c.9206T>C MANE Select	NP_055178.3:p.Leu3069Ser
NM_001278055.2:c.8765T>C	NP_001264984.1:p.Leu2922Ser