Canonical Allele Identifier: CA387539544

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23915716A>C (hg19) ; chr13:g.23341577A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341577A>C , CM000675.2:g.23341577A>C	GRCh38
NC_000013.10:g.23915716A>C , CM000675.1:g.23915716A>C	GRCh37
NC_000013.9:g.22813716A>C	NCBI36
NG_012342.1:g.97126T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+12208T>G	ENSP00000508399.1:n.2185+12208T>G
ENST00000682944.1:c.2326T>G	ENSP00000507173.1:p.Phe776Val
ENST00000683210.1:c.2185+12208T>G	ENSP00000506739.1:n.2185+12208T>G
ENST00000683270.1:c.2290T>G	ENSP00000507624.1:p.Phe764Val
ENST00000683367.1:c.2177-12093T>G	ENSP00000507780.1:n.2177-12093T>G
ENST00000683489.1:c.2291+8T>G	ENSP00000508403.1:n.2291+8T>G
ENST00000683680.1:c.2318+8T>G	ENSP00000507223.1:n.2318+8T>G
ENST00000684163.1:c.2203+5234T>G	ENSP00000508262.1:n.2203+5234T>G
ENST00000684196.1:n.4543-12093T>G
ENST00000684325.1:c.2185+12208T>G	ENSP00000508121.1:n.2185+12208T>G
ENST00000684385.1:c.2220+5234T>G	ENSP00000507855.1:n.2220+5234T>G
ENST00000684497.1:c.2185+12208T>G	ENSP00000507057.1:n.2185+12208T>G
ENST00000382292.9:c.2299T>G MANE Select	ENSP00000371729.3:p.Phe767Val
ENST00000423156.2:c.2186-12093T>G	ENSP00000390925.2:n.2186-12093T>G
ENST00000455470.6:c.2299T>G	ENSP00000406565.2:p.Phe767Val
ENST00000382292.7:c.2299T>G	ENSP00000371729.3:p.Phe767Val
ENST00000382298.7:c.2299T>G	ENSP00000371735.3:p.Phe767Val
ENST00000402364.1:c.49T>G	ENSP00000385844.1:p.Phe17Val
ENST00000423156.1:c.1058-12093T>G	ENSP00000390925.1:n.1058-12093T>G
ENST00000455470.5:c.1997T>G
NM_001278055.1:c.1858T>G	NP_001264984.1:p.Phe620Val
NM_014363.5:c.2299T>G	NP_055178.3:p.Phe767Val
XM_005266338.1:c.2326T>G	XP_005266395.1:p.Phe776Val
XM_011535038.1:c.2350T>G	XP_011533340.1:p.Phe784Val
XM_011535039.1:c.2317T>G	XP_011533341.1:p.Phe773Val
XM_005266338.2:c.2326T>G	XP_005266395.1:p.Phe776Val
XM_011535039.2:c.2317T>G	XP_011533341.1:p.Phe773Val
XM_017020539.1:c.2290T>G	XP_016876028.1:p.Phe764Val
XM_024449337.1:c.2326T>G	XP_024305105.1:p.Phe776Val
NM_014363.6:c.2299T>G MANE Select	NP_055178.3:p.Phe767Val
NM_001278055.2:c.1858T>G	NP_001264984.1:p.Phe620Val