Canonical Allele Identifier: CA6910682

Gene: SACS

Linked Data

• ClinVar Variation Id: 311515
• ClinVar RCV Id: RCV000315960 ; RCV001411302
• dbSNP Id: rs139670073
• ExAC: 13:23909025 C / T
• gnomAD v2: 13-23909025-C-T
• gnomAD v3: 13-23334886-C-T
• gnomAD v4: 13-23334886-C-T
• COSMIC: COSM2266134 ; COSM2266135
• MyVariant Identifiers: chr13:g.23909025C>T (hg19) ; chr13:g.23334886C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334886C>T , CM000675.2:g.23334886C>T	GRCh38
NC_000013.10:g.23909025C>T , CM000675.1:g.23909025C>T	GRCh37
NC_000013.9:g.22807025C>T	NCBI36
NG_012342.1:g.103817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18899G>A	ENSP00000508399.1:n.2185+18899G>A
ENST00000682944.1:c.9017G>A	ENSP00000507173.1:p.Arg3006Gln
ENST00000683210.1:c.2185+18899G>A	ENSP00000506739.1:n.2185+18899G>A
ENST00000683270.1:c.6445+2536G>A	ENSP00000507624.1:n.6445+2536G>A
ENST00000683367.1:c.2177-5402G>A	ENSP00000507780.1:n.2177-5402G>A
ENST00000683489.1:c.2292-4934G>A	ENSP00000508403.1:n.2292-4934G>A
ENST00000683680.1:c.2319-4934G>A	ENSP00000507223.1:n.2319-4934G>A
ENST00000684163.1:c.2204-5402G>A	ENSP00000508262.1:n.2204-5402G>A
ENST00000684196.1:n.4543-5402G>A
ENST00000684325.1:c.2186-13212G>A	ENSP00000508121.1:n.2186-13212G>A
ENST00000684385.1:c.2221-5402G>A	ENSP00000507855.1:n.2221-5402G>A
ENST00000684497.1:c.2186-12242G>A	ENSP00000507057.1:n.2186-12242G>A
ENST00000382292.9:c.8990G>A MANE Select	ENSP00000371729.3:p.Arg2997Gln
ENST00000423156.2:c.2186-5402G>A	ENSP00000390925.2:n.2186-5402G>A
ENST00000455470.6:c.2432-5402G>A	ENSP00000406565.2:n.2432-5402G>A
ENST00000382292.7:c.8990G>A	ENSP00000371729.3:p.Arg2997Gln
ENST00000382298.7:c.8990G>A	ENSP00000371735.3:p.Arg2997Gln
ENST00000402364.1:c.6740G>A	ENSP00000385844.1:p.Arg2247Gln
ENST00000423156.1:c.1058-5402G>A	ENSP00000390925.1:n.1058-5402G>A
ENST00000455470.5:c.2130-5402G>A
NM_001278055.1:c.8549G>A	NP_001264984.1:p.Arg2850Gln
NM_014363.5:c.8990G>A	NP_055178.3:p.Arg2997Gln
XM_005266338.1:c.9017G>A	XP_005266395.1:p.Arg3006Gln
XM_011535038.1:c.9041G>A	XP_011533340.1:p.Arg3014Gln
XM_011535039.1:c.9008G>A	XP_011533341.1:p.Arg3003Gln
XM_005266338.2:c.9017G>A	XP_005266395.1:p.Arg3006Gln
XM_011535039.2:c.9008G>A	XP_011533341.1:p.Arg3003Gln
XM_017020539.1:c.8981G>A	XP_016876028.1:p.Arg2994Gln
XM_024449337.1:c.9017G>A	XP_024305105.1:p.Arg3006Gln
NM_014363.6:c.8990G>A MANE Select	NP_055178.3:p.Arg2997Gln
NM_001278055.2:c.8549G>A	NP_001264984.1:p.Arg2850Gln