Canonical Allele Identifier: CA387505771

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23904811T>A (hg19) ; chr13:g.23330672T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330672T>A , CM000675.2:g.23330672T>A	GRCh38
NC_000013.10:g.23904811T>A , CM000675.1:g.23904811T>A	GRCh37
NC_000013.9:g.22802811T>A	NCBI36
NG_012342.1:g.108031A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-18557A>T	ENSP00000508399.1:n.2186-18557A>T
ENST00000682944.1:c.13231A>T	ENSP00000507173.1:p.Asn4411Tyr
ENST00000683210.1:c.2185+23113A>T	ENSP00000506739.1:n.2185+23113A>T
ENST00000683270.1:c.6446-1188A>T	ENSP00000507624.1:n.6446-1188A>T
ENST00000683367.1:c.2177-1188A>T	ENSP00000507780.1:n.2177-1188A>T
ENST00000683489.1:c.2292-720A>T	ENSP00000508403.1:n.2292-720A>T
ENST00000683680.1:c.2319-720A>T	ENSP00000507223.1:n.2319-720A>T
ENST00000684163.1:c.2204-1188A>T	ENSP00000508262.1:n.2204-1188A>T
ENST00000684196.1:n.4543-1188A>T
ENST00000684325.1:c.2186-8998A>T	ENSP00000508121.1:n.2186-8998A>T
ENST00000684385.1:c.2221-1188A>T	ENSP00000507855.1:n.2221-1188A>T
ENST00000684497.1:c.2186-8028A>T	ENSP00000507057.1:n.2186-8028A>T
ENST00000382292.9:c.13204A>T MANE Select	ENSP00000371729.3:p.Asn4402Tyr
ENST00000423156.2:c.2186-1188A>T	ENSP00000390925.2:n.2186-1188A>T
ENST00000455470.6:c.2432-1188A>T	ENSP00000406565.2:n.2432-1188A>T
ENST00000382292.7:c.13204A>T	ENSP00000371729.3:p.Asn4402Tyr
ENST00000382298.7:c.13204A>T	ENSP00000371735.3:p.Asn4402Tyr
ENST00000402364.1:c.10954A>T	ENSP00000385844.1:p.Asn3652Tyr
ENST00000423156.1:c.1058-1188A>T	ENSP00000390925.1:n.1058-1188A>T
ENST00000455470.5:c.2130-1188A>T
NM_001278055.1:c.12763A>T	NP_001264984.1:p.Asn4255Tyr
NM_014363.5:c.13204A>T	NP_055178.3:p.Asn4402Tyr
XM_005266338.1:c.13231A>T	XP_005266395.1:p.Asn4411Tyr
XM_011535038.1:c.13255A>T	XP_011533340.1:p.Asn4419Tyr
XM_011535039.1:c.13222A>T	XP_011533341.1:p.Asn4408Tyr
XM_005266338.2:c.13231A>T	XP_005266395.1:p.Asn4411Tyr
XM_011535039.2:c.13222A>T	XP_011533341.1:p.Asn4408Tyr
XM_017020539.1:c.13195A>T	XP_016876028.1:p.Asn4399Tyr
XM_024449337.1:c.13231A>T	XP_024305105.1:p.Asn4411Tyr
NM_014363.6:c.13204A>T MANE Select	NP_055178.3:p.Asn4402Tyr
NM_001278055.2:c.12763A>T	NP_001264984.1:p.Asn4255Tyr