Canonical Allele Identifier: CA387506223

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23905010T>G (hg19) ; chr13:g.23330871T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330871T>G , CM000675.2:g.23330871T>G	GRCh38
NC_000013.10:g.23905010T>G , CM000675.1:g.23905010T>G	GRCh37
NC_000013.9:g.22803010T>G	NCBI36
NG_012342.1:g.107832A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-18756A>C	ENSP00000508399.1:n.2186-18756A>C
ENST00000682944.1:c.13032A>C	ENSP00000507173.1:p.Lys4344Asn
ENST00000683210.1:c.2185+22914A>C	ENSP00000506739.1:n.2185+22914A>C
ENST00000683270.1:c.6446-1387A>C	ENSP00000507624.1:n.6446-1387A>C
ENST00000683367.1:c.2177-1387A>C	ENSP00000507780.1:n.2177-1387A>C
ENST00000683489.1:c.2292-919A>C	ENSP00000508403.1:n.2292-919A>C
ENST00000683680.1:c.2319-919A>C	ENSP00000507223.1:n.2319-919A>C
ENST00000684163.1:c.2204-1387A>C	ENSP00000508262.1:n.2204-1387A>C
ENST00000684196.1:n.4543-1387A>C
ENST00000684325.1:c.2186-9197A>C	ENSP00000508121.1:n.2186-9197A>C
ENST00000684385.1:c.2221-1387A>C	ENSP00000507855.1:n.2221-1387A>C
ENST00000684497.1:c.2186-8227A>C	ENSP00000507057.1:n.2186-8227A>C
ENST00000382292.9:c.13005A>C MANE Select	ENSP00000371729.3:p.Lys4335Asn
ENST00000423156.2:c.2186-1387A>C	ENSP00000390925.2:n.2186-1387A>C
ENST00000455470.6:c.2432-1387A>C	ENSP00000406565.2:n.2432-1387A>C
ENST00000382292.7:c.13005A>C	ENSP00000371729.3:p.Lys4335Asn
ENST00000382298.7:c.13005A>C	ENSP00000371735.3:p.Lys4335Asn
ENST00000402364.1:c.10755A>C	ENSP00000385844.1:p.Lys3585Asn
ENST00000423156.1:c.1058-1387A>C	ENSP00000390925.1:n.1058-1387A>C
ENST00000455470.5:c.2130-1387A>C
NM_001278055.1:c.12564A>C	NP_001264984.1:p.Lys4188Asn
NM_014363.5:c.13005A>C	NP_055178.3:p.Lys4335Asn
XM_005266338.1:c.13032A>C	XP_005266395.1:p.Lys4344Asn
XM_011535038.1:c.13056A>C	XP_011533340.1:p.Lys4352Asn
XM_011535039.1:c.13023A>C	XP_011533341.1:p.Lys4341Asn
XM_005266338.2:c.13032A>C	XP_005266395.1:p.Lys4344Asn
XM_011535039.2:c.13023A>C	XP_011533341.1:p.Lys4341Asn
XM_017020539.1:c.12996A>C	XP_016876028.1:p.Lys4332Asn
XM_024449337.1:c.13032A>C	XP_024305105.1:p.Lys4344Asn
NM_014363.6:c.13005A>C MANE Select	NP_055178.3:p.Lys4335Asn
NM_001278055.2:c.12564A>C	NP_001264984.1:p.Lys4188Asn