Canonical Allele Identifier: CA387513354

Gene: SACS

Linked Data

• dbSNP Id: rs761501767
• MyVariant Identifiers: chr13:g.23908089A>C (hg19) ; chr13:g.23333950A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333950A>C , CM000675.2:g.23333950A>C	GRCh38
NC_000013.10:g.23908089A>C , CM000675.1:g.23908089A>C	GRCh37
NC_000013.9:g.22806089A>C	NCBI36
NG_012342.1:g.104753T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+19835T>G	ENSP00000508399.1:n.2185+19835T>G
ENST00000682944.1:c.9953T>G	ENSP00000507173.1:p.Ile3318Ser
ENST00000683210.1:c.2185+19835T>G	ENSP00000506739.1:n.2185+19835T>G
ENST00000683270.1:c.6445+3472T>G	ENSP00000507624.1:n.6445+3472T>G
ENST00000683367.1:c.2177-4466T>G	ENSP00000507780.1:n.2177-4466T>G
ENST00000683489.1:c.2292-3998T>G	ENSP00000508403.1:n.2292-3998T>G
ENST00000683680.1:c.2319-3998T>G	ENSP00000507223.1:n.2319-3998T>G
ENST00000684163.1:c.2204-4466T>G	ENSP00000508262.1:n.2204-4466T>G
ENST00000684196.1:n.4543-4466T>G
ENST00000684325.1:c.2186-12276T>G	ENSP00000508121.1:n.2186-12276T>G
ENST00000684385.1:c.2221-4466T>G	ENSP00000507855.1:n.2221-4466T>G
ENST00000684497.1:c.2186-11306T>G	ENSP00000507057.1:n.2186-11306T>G
ENST00000382292.9:c.9926T>G MANE Select	ENSP00000371729.3:p.Ile3309Ser
ENST00000423156.2:c.2186-4466T>G	ENSP00000390925.2:n.2186-4466T>G
ENST00000455470.6:c.2432-4466T>G	ENSP00000406565.2:n.2432-4466T>G
ENST00000382292.7:c.9926T>G	ENSP00000371729.3:p.Ile3309Ser
ENST00000382298.7:c.9926T>G	ENSP00000371735.3:p.Ile3309Ser
ENST00000402364.1:c.7676T>G	ENSP00000385844.1:p.Ile2559Ser
ENST00000423156.1:c.1058-4466T>G	ENSP00000390925.1:n.1058-4466T>G
ENST00000455470.5:c.2130-4466T>G
NM_001278055.1:c.9485T>G	NP_001264984.1:p.Ile3162Ser
NM_014363.5:c.9926T>G	NP_055178.3:p.Ile3309Ser
XM_005266338.1:c.9953T>G	XP_005266395.1:p.Ile3318Ser
XM_011535038.1:c.9977T>G	XP_011533340.1:p.Ile3326Ser
XM_011535039.1:c.9944T>G	XP_011533341.1:p.Ile3315Ser
XM_005266338.2:c.9953T>G	XP_005266395.1:p.Ile3318Ser
XM_011535039.2:c.9944T>G	XP_011533341.1:p.Ile3315Ser
XM_017020539.1:c.9917T>G	XP_016876028.1:p.Ile3306Ser
XM_024449337.1:c.9953T>G	XP_024305105.1:p.Ile3318Ser
NM_014363.6:c.9926T>G MANE Select	NP_055178.3:p.Ile3309Ser
NM_001278055.2:c.9485T>G	NP_001264984.1:p.Ile3162Ser