Canonical Allele Identifier: CA6910122

Gene: SACS

Linked Data

• dbSNP Id: rs746486693
• ExAC: 13:23905398 A / G
• gnomAD v2: 13-23905398-A-G
• gnomAD v4: 13-23331259-A-G
• MyVariant Identifiers: chr13:g.23905398A>G (hg19) ; chr13:g.23331259A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23331259A>G , CM000675.2:g.23331259A>G	GRCh38
NC_000013.10:g.23905398A>G , CM000675.1:g.23905398A>G	GRCh37
NC_000013.9:g.22803398A>G	NCBI36
NG_012342.1:g.107444T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-19144T>C	ENSP00000508399.1:n.2186-19144T>C
ENST00000682944.1:c.12644T>C	ENSP00000507173.1:p.Ile4215Thr
ENST00000683210.1:c.2185+22526T>C	ENSP00000506739.1:n.2185+22526T>C
ENST00000683270.1:c.6446-1775T>C	ENSP00000507624.1:n.6446-1775T>C
ENST00000683367.1:c.2177-1775T>C	ENSP00000507780.1:n.2177-1775T>C
ENST00000683489.1:c.2292-1307T>C	ENSP00000508403.1:n.2292-1307T>C
ENST00000683680.1:c.2319-1307T>C	ENSP00000507223.1:n.2319-1307T>C
ENST00000684163.1:c.2204-1775T>C	ENSP00000508262.1:n.2204-1775T>C
ENST00000684196.1:n.4543-1775T>C
ENST00000684325.1:c.2186-9585T>C	ENSP00000508121.1:n.2186-9585T>C
ENST00000684385.1:c.2221-1775T>C	ENSP00000507855.1:n.2221-1775T>C
ENST00000684497.1:c.2186-8615T>C	ENSP00000507057.1:n.2186-8615T>C
ENST00000382292.9:c.12617T>C MANE Select	ENSP00000371729.3:p.Ile4206Thr
ENST00000423156.2:c.2186-1775T>C	ENSP00000390925.2:n.2186-1775T>C
ENST00000455470.6:c.2432-1775T>C	ENSP00000406565.2:n.2432-1775T>C
ENST00000382292.7:c.12617T>C	ENSP00000371729.3:p.Ile4206Thr
ENST00000382298.7:c.12617T>C	ENSP00000371735.3:p.Ile4206Thr
ENST00000402364.1:c.10367T>C	ENSP00000385844.1:p.Ile3456Thr
ENST00000423156.1:c.1058-1775T>C	ENSP00000390925.1:n.1058-1775T>C
ENST00000455470.5:c.2130-1775T>C
NM_001278055.1:c.12176T>C	NP_001264984.1:p.Ile4059Thr
NM_014363.5:c.12617T>C	NP_055178.3:p.Ile4206Thr
XM_005266338.1:c.12644T>C	XP_005266395.1:p.Ile4215Thr
XM_011535038.1:c.12668T>C	XP_011533340.1:p.Ile4223Thr
XM_011535039.1:c.12635T>C	XP_011533341.1:p.Ile4212Thr
XM_005266338.2:c.12644T>C	XP_005266395.1:p.Ile4215Thr
XM_011535039.2:c.12635T>C	XP_011533341.1:p.Ile4212Thr
XM_017020539.1:c.12608T>C	XP_016876028.1:p.Ile4203Thr
XM_024449337.1:c.12644T>C	XP_024305105.1:p.Ile4215Thr
NM_014363.6:c.12617T>C MANE Select	NP_055178.3:p.Ile4206Thr
NM_001278055.2:c.12176T>C	NP_001264984.1:p.Ile4059Thr