Canonical Allele Identifier: CA483159964

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909168A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23335029A>G , CM000675.2:g.23335029A>G	GRCh38
NC_000013.10:g.23909168A>G , CM000675.1:g.23909168A>G	GRCh37
NC_000013.9:g.22807168A>G	NCBI36
NG_012342.1:g.103674T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18756T>C	ENSP00000508399.1:n.2185+18756T>C
ENST00000682944.1:c.8874T>C	ENSP00000507173.1:p.Ile2958=
ENST00000683210.1:c.2185+18756T>C	ENSP00000506739.1:n.2185+18756T>C
ENST00000683270.1:c.6445+2393T>C	ENSP00000507624.1:n.6445+2393T>C
ENST00000683367.1:c.2177-5545T>C	ENSP00000507780.1:n.2177-5545T>C
ENST00000683489.1:c.2292-5077T>C	ENSP00000508403.1:n.2292-5077T>C
ENST00000683680.1:c.2319-5077T>C	ENSP00000507223.1:n.2319-5077T>C
ENST00000684163.1:c.2204-5545T>C	ENSP00000508262.1:n.2204-5545T>C
ENST00000684196.1:n.4543-5545T>C
ENST00000684325.1:c.2186-13355T>C	ENSP00000508121.1:n.2186-13355T>C
ENST00000684385.1:c.2221-5545T>C	ENSP00000507855.1:n.2221-5545T>C
ENST00000684497.1:c.2186-12385T>C	ENSP00000507057.1:n.2186-12385T>C
ENST00000382292.9:c.8847T>C MANE Select	ENSP00000371729.3:p.Ile2949=
ENST00000423156.2:c.2186-5545T>C	ENSP00000390925.2:n.2186-5545T>C
ENST00000455470.6:c.2432-5545T>C	ENSP00000406565.2:n.2432-5545T>C
ENST00000382292.7:c.8847T>C	ENSP00000371729.3:p.Ile2949=
ENST00000382298.7:c.8847T>C	ENSP00000371735.3:p.Ile2949=
ENST00000402364.1:c.6597T>C	ENSP00000385844.1:p.Ile2199=
ENST00000423156.1:c.1058-5545T>C	ENSP00000390925.1:n.1058-5545T>C
ENST00000455470.5:c.2130-5545T>C
NM_001278055.1:c.8406T>C	NP_001264984.1:p.Ile2802=
NM_014363.5:c.8847T>C	NP_055178.3:p.Ile2949=
XM_005266338.1:c.8874T>C	XP_005266395.1:p.Ile2958=
XM_011535038.1:c.8898T>C	XP_011533340.1:p.Ile2966=
XM_011535039.1:c.8865T>C	XP_011533341.1:p.Ile2955=
XM_005266338.2:c.8874T>C	XP_005266395.1:p.Ile2958=
XM_011535039.2:c.8865T>C	XP_011533341.1:p.Ile2955=
XM_017020539.1:c.8838T>C	XP_016876028.1:p.Ile2946=
XM_024449337.1:c.8874T>C	XP_024305105.1:p.Ile2958=
NM_014363.6:c.8847T>C MANE Select	NP_055178.3:p.Ile2949=
NM_001278055.2:c.8406T>C	NP_001264984.1:p.Ile2802=