Canonical Allele Identifier: CA387504898

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23904414A>G (hg19) ; chr13:g.23330275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330275A>G , CM000675.2:g.23330275A>G	GRCh38
NC_000013.10:g.23904414A>G , CM000675.1:g.23904414A>G	GRCh37
NC_000013.9:g.22802414A>G	NCBI36
NG_012342.1:g.108428T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18160T>C	ENSP00000508399.1:n.2186-18160T>C
ENST00000682944.1:c.13628T>C	ENSP00000507173.1:p.Leu4543Ser
ENST00000683210.1:c.2185+23510T>C	ENSP00000506739.1:n.2185+23510T>C
ENST00000683270.1:c.6446-791T>C	ENSP00000507624.1:n.6446-791T>C
ENST00000683367.1:c.2177-791T>C	ENSP00000507780.1:n.2177-791T>C
ENST00000683489.1:c.2292-323T>C	ENSP00000508403.1:n.2292-323T>C
ENST00000683680.1:c.2319-323T>C	ENSP00000507223.1:n.2319-323T>C
ENST00000684163.1:c.2204-791T>C	ENSP00000508262.1:n.2204-791T>C
ENST00000684196.1:n.4543-791T>C
ENST00000684325.1:c.2186-8601T>C	ENSP00000508121.1:n.2186-8601T>C
ENST00000684385.1:c.2221-791T>C	ENSP00000507855.1:n.2221-791T>C
ENST00000684497.1:c.2186-7631T>C	ENSP00000507057.1:n.2186-7631T>C
ENST00000382292.9:c.13601T>C MANE Select	ENSP00000371729.3:p.Leu4534Ser
ENST00000423156.2:c.2186-791T>C	ENSP00000390925.2:n.2186-791T>C
ENST00000455470.6:c.2432-791T>C	ENSP00000406565.2:n.2432-791T>C
ENST00000382292.7:c.13601T>C	ENSP00000371729.3:p.Leu4534Ser
ENST00000382298.7:c.13601T>C	ENSP00000371735.3:p.Leu4534Ser
ENST00000402364.1:c.11351T>C	ENSP00000385844.1:p.Leu3784Ser
ENST00000423156.1:c.1058-791T>C	ENSP00000390925.1:n.1058-791T>C
ENST00000455470.5:c.2130-791T>C
NM_001278055.1:c.13160T>C	NP_001264984.1:p.Leu4387Ser
NM_014363.5:c.13601T>C	NP_055178.3:p.Leu4534Ser
XM_005266338.1:c.13628T>C	XP_005266395.1:p.Leu4543Ser
XM_011535038.1:c.13652T>C	XP_011533340.1:p.Leu4551Ser
XM_011535039.1:c.13619T>C	XP_011533341.1:p.Leu4540Ser
XM_005266338.2:c.13628T>C	XP_005266395.1:p.Leu4543Ser
XM_011535039.2:c.13619T>C	XP_011533341.1:p.Leu4540Ser
XM_017020539.1:c.13592T>C	XP_016876028.1:p.Leu4531Ser
XM_024449337.1:c.13628T>C	XP_024305105.1:p.Leu4543Ser
NM_014363.6:c.13601T>C MANE Select	NP_055178.3:p.Leu4534Ser
NM_001278055.2:c.13160T>C	NP_001264984.1:p.Leu4387Ser