Canonical Allele Identifier: CA387540532

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23915775A>C (hg19) ; chr13:g.23341636A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341636A>C , CM000675.2:g.23341636A>C	GRCh38
NC_000013.10:g.23915775A>C , CM000675.1:g.23915775A>C	GRCh37
NC_000013.9:g.22813775A>C	NCBI36
NG_012342.1:g.97067T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12149T>G	ENSP00000508399.1:n.2185+12149T>G
ENST00000682944.1:c.2267T>G	ENSP00000507173.1:p.Ile756Ser
ENST00000683210.1:c.2185+12149T>G	ENSP00000506739.1:n.2185+12149T>G
ENST00000683270.1:c.2231T>G	ENSP00000507624.1:p.Ile744Ser
ENST00000683367.1:c.2176+12149T>G	ENSP00000507780.1:n.2176+12149T>G
ENST00000683489.1:c.2240T>G	ENSP00000508403.1:p.Ile747Ser
ENST00000683680.1:c.2267T>G	ENSP00000507223.1:p.Ile756Ser
ENST00000684163.1:c.2203+5175T>G	ENSP00000508262.1:n.2203+5175T>G
ENST00000684196.1:n.4542+12149T>G
ENST00000684325.1:c.2185+12149T>G	ENSP00000508121.1:n.2185+12149T>G
ENST00000684385.1:c.2220+5175T>G	ENSP00000507855.1:n.2220+5175T>G
ENST00000684497.1:c.2185+12149T>G	ENSP00000507057.1:n.2185+12149T>G
ENST00000382292.9:c.2240T>G MANE Select	ENSP00000371729.3:p.Ile747Ser
ENST00000423156.2:c.2185+12149T>G	ENSP00000390925.2:n.2185+12149T>G
ENST00000455470.6:c.2240T>G	ENSP00000406565.2:p.Ile747Ser
ENST00000382292.7:c.2240T>G	ENSP00000371729.3:p.Ile747Ser
ENST00000382298.7:c.2240T>G	ENSP00000371735.3:p.Ile747Ser
ENST00000402364.1:c.-11T>G	ENSP00000385844.1:n.-11T>G
ENST00000423156.1:c.1057+12149T>G	ENSP00000390925.1:n.1057+12149T>G
ENST00000455470.5:c.1938T>G
NM_001278055.1:c.1799T>G	NP_001264984.1:p.Ile600Ser
NM_014363.5:c.2240T>G	NP_055178.3:p.Ile747Ser
XM_005266338.1:c.2267T>G	XP_005266395.1:p.Ile756Ser
XM_011535038.1:c.2291T>G	XP_011533340.1:p.Ile764Ser
XM_011535039.1:c.2258T>G	XP_011533341.1:p.Ile753Ser
XM_005266338.2:c.2267T>G	XP_005266395.1:p.Ile756Ser
XM_011535039.2:c.2258T>G	XP_011533341.1:p.Ile753Ser
XM_017020539.1:c.2231T>G	XP_016876028.1:p.Ile744Ser
XM_024449337.1:c.2267T>G	XP_024305105.1:p.Ile756Ser
NM_014363.6:c.2240T>G MANE Select	NP_055178.3:p.Ile747Ser
NM_001278055.2:c.1799T>G	NP_001264984.1:p.Ile600Ser