Canonical Allele Identifier: CA483157251

Gene: SACS

Linked Data

• gnomAD v4: 13-23330235-G-T
• MyVariant Identifiers: chr13:g.23904374G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330235G>T , CM000675.2:g.23330235G>T	GRCh38
NC_000013.10:g.23904374G>T , CM000675.1:g.23904374G>T	GRCh37
NC_000013.9:g.22802374G>T	NCBI36
NG_012342.1:g.108468C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18120C>A	ENSP00000508399.1:n.2186-18120C>A
ENST00000682944.1:c.13668C>A	ENSP00000507173.1:p.Ile4556=
ENST00000683210.1:c.2185+23550C>A	ENSP00000506739.1:n.2185+23550C>A
ENST00000683270.1:c.6446-751C>A	ENSP00000507624.1:n.6446-751C>A
ENST00000683367.1:c.2177-751C>A	ENSP00000507780.1:n.2177-751C>A
ENST00000683489.1:c.2292-283C>A	ENSP00000508403.1:n.2292-283C>A
ENST00000683680.1:c.2319-283C>A	ENSP00000507223.1:n.2319-283C>A
ENST00000684163.1:c.2204-751C>A	ENSP00000508262.1:n.2204-751C>A
ENST00000684196.1:n.4543-751C>A
ENST00000684325.1:c.2186-8561C>A	ENSP00000508121.1:n.2186-8561C>A
ENST00000684385.1:c.2221-751C>A	ENSP00000507855.1:n.2221-751C>A
ENST00000684497.1:c.2186-7591C>A	ENSP00000507057.1:n.2186-7591C>A
ENST00000382292.9:c.13641C>A MANE Select	ENSP00000371729.3:p.Ile4547=
ENST00000423156.2:c.2186-751C>A	ENSP00000390925.2:n.2186-751C>A
ENST00000455470.6:c.2432-751C>A	ENSP00000406565.2:n.2432-751C>A
ENST00000382292.7:c.13641C>A	ENSP00000371729.3:p.Ile4547=
ENST00000382298.7:c.13641C>A	ENSP00000371735.3:p.Ile4547=
ENST00000402364.1:c.11391C>A	ENSP00000385844.1:p.Ile3797=
ENST00000423156.1:c.1058-751C>A	ENSP00000390925.1:n.1058-751C>A
ENST00000455470.5:c.2130-751C>A
NM_001278055.1:c.13200C>A	NP_001264984.1:p.Ile4400=
NM_014363.5:c.13641C>A	NP_055178.3:p.Ile4547=
XM_005266338.1:c.13668C>A	XP_005266395.1:p.Ile4556=
XM_011535038.1:c.13692C>A	XP_011533340.1:p.Ile4564=
XM_011535039.1:c.13659C>A	XP_011533341.1:p.Ile4553=
XM_005266338.2:c.13668C>A	XP_005266395.1:p.Ile4556=
XM_011535039.2:c.13659C>A	XP_011533341.1:p.Ile4553=
XM_017020539.1:c.13632C>A	XP_016876028.1:p.Ile4544=
XM_024449337.1:c.13668C>A	XP_024305105.1:p.Ile4556=
NM_014363.6:c.13641C>A MANE Select	NP_055178.3:p.Ile4547=
NM_001278055.2:c.13200C>A	NP_001264984.1:p.Ile4400=