Canonical Allele Identifier: CA387521071

Gene: SACS

Linked Data

• gnomAD v4: 13-23337229-A-C
• MyVariant Identifiers: chr13:g.23911368A>C (hg19) ; chr13:g.23337229A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337229A>C , CM000675.2:g.23337229A>C	GRCh38
NC_000013.10:g.23911368A>C , CM000675.1:g.23911368A>C	GRCh37
NC_000013.9:g.22809368A>C	NCBI36
NG_012342.1:g.101474T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16556T>G	ENSP00000508399.1:n.2185+16556T>G
ENST00000682944.1:c.6674T>G	ENSP00000507173.1:p.Leu2225Arg
ENST00000683210.1:c.2185+16556T>G	ENSP00000506739.1:n.2185+16556T>G
ENST00000683270.1:c.6445+193T>G	ENSP00000507624.1:n.6445+193T>G
ENST00000683367.1:c.2177-7745T>G	ENSP00000507780.1:n.2177-7745T>G
ENST00000683489.1:c.2291+4356T>G	ENSP00000508403.1:n.2291+4356T>G
ENST00000683680.1:c.2318+4356T>G	ENSP00000507223.1:n.2318+4356T>G
ENST00000684163.1:c.2204-7745T>G	ENSP00000508262.1:n.2204-7745T>G
ENST00000684196.1:n.4543-7745T>G
ENST00000684325.1:c.2186-15555T>G	ENSP00000508121.1:n.2186-15555T>G
ENST00000684385.1:c.2221-7745T>G	ENSP00000507855.1:n.2221-7745T>G
ENST00000684497.1:c.2186-14585T>G	ENSP00000507057.1:n.2186-14585T>G
ENST00000382292.9:c.6647T>G MANE Select	ENSP00000371729.3:p.Leu2216Arg
ENST00000423156.2:c.2186-7745T>G	ENSP00000390925.2:n.2186-7745T>G
ENST00000455470.6:c.2431+4216T>G	ENSP00000406565.2:n.2431+4216T>G
ENST00000382292.7:c.6647T>G	ENSP00000371729.3:p.Leu2216Arg
ENST00000382298.7:c.6647T>G	ENSP00000371735.3:p.Leu2216Arg
ENST00000402364.1:c.4397T>G	ENSP00000385844.1:p.Leu1466Arg
ENST00000423156.1:c.1058-7745T>G	ENSP00000390925.1:n.1058-7745T>G
ENST00000455470.5:c.2129+4216T>G
NM_001278055.1:c.6206T>G	NP_001264984.1:p.Leu2069Arg
NM_014363.5:c.6647T>G	NP_055178.3:p.Leu2216Arg
XM_005266338.1:c.6674T>G	XP_005266395.1:p.Leu2225Arg
XM_011535038.1:c.6698T>G	XP_011533340.1:p.Leu2233Arg
XM_011535039.1:c.6665T>G	XP_011533341.1:p.Leu2222Arg
XM_005266338.2:c.6674T>G	XP_005266395.1:p.Leu2225Arg
XM_011535039.2:c.6665T>G	XP_011533341.1:p.Leu2222Arg
XM_017020539.1:c.6638T>G	XP_016876028.1:p.Leu2213Arg
XM_024449337.1:c.6674T>G	XP_024305105.1:p.Leu2225Arg
NM_014363.6:c.6647T>G MANE Select	NP_055178.3:p.Leu2216Arg
NM_001278055.2:c.6206T>G	NP_001264984.1:p.Leu2069Arg