Canonical Allele Identifier: CA387540558

Gene: SACS

Linked Data

• gnomAD v4: 13-23341651-C-A
• MyVariant Identifiers: chr13:g.23915790C>A (hg19) ; chr13:g.23341651C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341651C>A , CM000675.2:g.23341651C>A	GRCh38
NC_000013.10:g.23915790C>A , CM000675.1:g.23915790C>A	GRCh37
NC_000013.9:g.22813790C>A	NCBI36
NG_012342.1:g.97052G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12134G>T	ENSP00000508399.1:n.2185+12134G>T
ENST00000682944.1:c.2252G>T	ENSP00000507173.1:p.Arg751Leu
ENST00000683210.1:c.2185+12134G>T	ENSP00000506739.1:n.2185+12134G>T
ENST00000683270.1:c.2216G>T	ENSP00000507624.1:p.Arg739Leu
ENST00000683367.1:c.2176+12134G>T	ENSP00000507780.1:n.2176+12134G>T
ENST00000683489.1:c.2225G>T	ENSP00000508403.1:p.Arg742Leu
ENST00000683680.1:c.2252G>T	ENSP00000507223.1:p.Arg751Leu
ENST00000684163.1:c.2203+5160G>T	ENSP00000508262.1:n.2203+5160G>T
ENST00000684196.1:n.4542+12134G>T
ENST00000684325.1:c.2185+12134G>T	ENSP00000508121.1:n.2185+12134G>T
ENST00000684385.1:c.2220+5160G>T	ENSP00000507855.1:n.2220+5160G>T
ENST00000684497.1:c.2185+12134G>T	ENSP00000507057.1:n.2185+12134G>T
ENST00000382292.9:c.2225G>T MANE Select	ENSP00000371729.3:p.Arg742Leu
ENST00000423156.2:c.2185+12134G>T	ENSP00000390925.2:n.2185+12134G>T
ENST00000455470.6:c.2225G>T	ENSP00000406565.2:p.Arg742Leu
ENST00000382292.7:c.2225G>T	ENSP00000371729.3:p.Arg742Leu
ENST00000382298.7:c.2225G>T	ENSP00000371735.3:p.Arg742Leu
ENST00000402364.1:c.-26G>T	ENSP00000385844.1:n.-26G>T
ENST00000423156.1:c.1057+12134G>T	ENSP00000390925.1:n.1057+12134G>T
ENST00000455470.5:c.1923G>T
NM_001278055.1:c.1784G>T	NP_001264984.1:p.Arg595Leu
NM_014363.5:c.2225G>T	NP_055178.3:p.Arg742Leu
XM_005266338.1:c.2252G>T	XP_005266395.1:p.Arg751Leu
XM_011535038.1:c.2276G>T	XP_011533340.1:p.Arg759Leu
XM_011535039.1:c.2243G>T	XP_011533341.1:p.Arg748Leu
XM_005266338.2:c.2252G>T	XP_005266395.1:p.Arg751Leu
XM_011535039.2:c.2243G>T	XP_011533341.1:p.Arg748Leu
XM_017020539.1:c.2216G>T	XP_016876028.1:p.Arg739Leu
XM_024449337.1:c.2252G>T	XP_024305105.1:p.Arg751Leu
NM_014363.6:c.2225G>T MANE Select	NP_055178.3:p.Arg742Leu
NM_001278055.2:c.1784G>T	NP_001264984.1:p.Arg595Leu