Canonical Allele Identifier: CA387504864

Gene: SACS

Linked Data

• ClinVar Variation Id: 496951
• ClinVar RCV Id: RCV000593641 ; RCV003465330
• dbSNP Id: rs1555249106
• gnomAD v4: 13-23330261-G-A
• MyVariant Identifiers: chr13:g.23904400G>A (hg19) ; chr13:g.23330261G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330261G>A , CM000675.2:g.23330261G>A	GRCh38
NC_000013.10:g.23904400G>A , CM000675.1:g.23904400G>A	GRCh37
NC_000013.9:g.22802400G>A	NCBI36
NG_012342.1:g.108442C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18146C>T	ENSP00000508399.1:n.2186-18146C>T
ENST00000682944.1:c.13642C>T	ENSP00000507173.1:p.Pro4548Ser
ENST00000683210.1:c.2185+23524C>T	ENSP00000506739.1:n.2185+23524C>T
ENST00000683270.1:c.6446-777C>T	ENSP00000507624.1:n.6446-777C>T
ENST00000683367.1:c.2177-777C>T	ENSP00000507780.1:n.2177-777C>T
ENST00000683489.1:c.2292-309C>T	ENSP00000508403.1:n.2292-309C>T
ENST00000683680.1:c.2319-309C>T	ENSP00000507223.1:n.2319-309C>T
ENST00000684163.1:c.2204-777C>T	ENSP00000508262.1:n.2204-777C>T
ENST00000684196.1:n.4543-777C>T
ENST00000684325.1:c.2186-8587C>T	ENSP00000508121.1:n.2186-8587C>T
ENST00000684385.1:c.2221-777C>T	ENSP00000507855.1:n.2221-777C>T
ENST00000684497.1:c.2186-7617C>T	ENSP00000507057.1:n.2186-7617C>T
ENST00000382292.9:c.13615C>T MANE Select	ENSP00000371729.3:p.Pro4539Ser
ENST00000423156.2:c.2186-777C>T	ENSP00000390925.2:n.2186-777C>T
ENST00000455470.6:c.2432-777C>T	ENSP00000406565.2:n.2432-777C>T
ENST00000382292.7:c.13615C>T	ENSP00000371729.3:p.Pro4539Ser
ENST00000382298.7:c.13615C>T	ENSP00000371735.3:p.Pro4539Ser
ENST00000402364.1:c.11365C>T	ENSP00000385844.1:p.Pro3789Ser
ENST00000423156.1:c.1058-777C>T	ENSP00000390925.1:n.1058-777C>T
ENST00000455470.5:c.2130-777C>T
NM_001278055.1:c.13174C>T	NP_001264984.1:p.Pro4392Ser
NM_014363.5:c.13615C>T	NP_055178.3:p.Pro4539Ser
XM_005266338.1:c.13642C>T	XP_005266395.1:p.Pro4548Ser
XM_011535038.1:c.13666C>T	XP_011533340.1:p.Pro4556Ser
XM_011535039.1:c.13633C>T	XP_011533341.1:p.Pro4545Ser
XM_005266338.2:c.13642C>T	XP_005266395.1:p.Pro4548Ser
XM_011535039.2:c.13633C>T	XP_011533341.1:p.Pro4545Ser
XM_017020539.1:c.13606C>T	XP_016876028.1:p.Pro4536Ser
XM_024449337.1:c.13642C>T	XP_024305105.1:p.Pro4548Ser
NM_014363.6:c.13615C>T MANE Select	NP_055178.3:p.Pro4539Ser
NM_001278055.2:c.13174C>T	NP_001264984.1:p.Pro4392Ser