Canonical Allele Identifier: CA483159935

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909033A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334894A>C , CM000675.2:g.23334894A>C	GRCh38
NC_000013.10:g.23909033A>C , CM000675.1:g.23909033A>C	GRCh37
NC_000013.9:g.22807033A>C	NCBI36
NG_012342.1:g.103809T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18891T>G	ENSP00000508399.1:n.2185+18891T>G
ENST00000682944.1:c.9009T>G	ENSP00000507173.1:p.Pro3003=
ENST00000683210.1:c.2185+18891T>G	ENSP00000506739.1:n.2185+18891T>G
ENST00000683270.1:c.6445+2528T>G	ENSP00000507624.1:n.6445+2528T>G
ENST00000683367.1:c.2177-5410T>G	ENSP00000507780.1:n.2177-5410T>G
ENST00000683489.1:c.2292-4942T>G	ENSP00000508403.1:n.2292-4942T>G
ENST00000683680.1:c.2319-4942T>G	ENSP00000507223.1:n.2319-4942T>G
ENST00000684163.1:c.2204-5410T>G	ENSP00000508262.1:n.2204-5410T>G
ENST00000684196.1:n.4543-5410T>G
ENST00000684325.1:c.2186-13220T>G	ENSP00000508121.1:n.2186-13220T>G
ENST00000684385.1:c.2221-5410T>G	ENSP00000507855.1:n.2221-5410T>G
ENST00000684497.1:c.2186-12250T>G	ENSP00000507057.1:n.2186-12250T>G
ENST00000382292.9:c.8982T>G MANE Select	ENSP00000371729.3:p.Pro2994=
ENST00000423156.2:c.2186-5410T>G	ENSP00000390925.2:n.2186-5410T>G
ENST00000455470.6:c.2432-5410T>G	ENSP00000406565.2:n.2432-5410T>G
ENST00000382292.7:c.8982T>G	ENSP00000371729.3:p.Pro2994=
ENST00000382298.7:c.8982T>G	ENSP00000371735.3:p.Pro2994=
ENST00000402364.1:c.6732T>G	ENSP00000385844.1:p.Pro2244=
ENST00000423156.1:c.1058-5410T>G	ENSP00000390925.1:n.1058-5410T>G
ENST00000455470.5:c.2130-5410T>G
NM_001278055.1:c.8541T>G	NP_001264984.1:p.Pro2847=
NM_014363.5:c.8982T>G	NP_055178.3:p.Pro2994=
XM_005266338.1:c.9009T>G	XP_005266395.1:p.Pro3003=
XM_011535038.1:c.9033T>G	XP_011533340.1:p.Pro3011=
XM_011535039.1:c.9000T>G	XP_011533341.1:p.Pro3000=
XM_005266338.2:c.9009T>G	XP_005266395.1:p.Pro3003=
XM_011535039.2:c.9000T>G	XP_011533341.1:p.Pro3000=
XM_017020539.1:c.8973T>G	XP_016876028.1:p.Pro2991=
XM_024449337.1:c.9009T>G	XP_024305105.1:p.Pro3003=
NM_014363.6:c.8982T>G MANE Select	NP_055178.3:p.Pro2994=
NM_001278055.2:c.8541T>G	NP_001264984.1:p.Pro2847=