Canonical Allele Identifier: CA387516336

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909442G>A (hg19) ; chr13:g.23335303G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23335303G>A , CM000675.2:g.23335303G>A	GRCh38
NC_000013.10:g.23909442G>A , CM000675.1:g.23909442G>A	GRCh37
NC_000013.9:g.22807442G>A	NCBI36
NG_012342.1:g.103400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18482C>T	ENSP00000508399.1:n.2185+18482C>T
ENST00000682944.1:c.8600C>T	ENSP00000507173.1:p.Thr2867Ile
ENST00000683210.1:c.2185+18482C>T	ENSP00000506739.1:n.2185+18482C>T
ENST00000683270.1:c.6445+2119C>T	ENSP00000507624.1:n.6445+2119C>T
ENST00000683367.1:c.2177-5819C>T	ENSP00000507780.1:n.2177-5819C>T
ENST00000683489.1:c.2292-5351C>T	ENSP00000508403.1:n.2292-5351C>T
ENST00000683680.1:c.2319-5351C>T	ENSP00000507223.1:n.2319-5351C>T
ENST00000684163.1:c.2204-5819C>T	ENSP00000508262.1:n.2204-5819C>T
ENST00000684196.1:n.4543-5819C>T
ENST00000684325.1:c.2186-13629C>T	ENSP00000508121.1:n.2186-13629C>T
ENST00000684385.1:c.2221-5819C>T	ENSP00000507855.1:n.2221-5819C>T
ENST00000684497.1:c.2186-12659C>T	ENSP00000507057.1:n.2186-12659C>T
ENST00000382292.9:c.8573C>T MANE Select	ENSP00000371729.3:p.Thr2858Ile
ENST00000423156.2:c.2186-5819C>T	ENSP00000390925.2:n.2186-5819C>T
ENST00000455470.6:c.2432-5819C>T	ENSP00000406565.2:n.2432-5819C>T
ENST00000382292.7:c.8573C>T	ENSP00000371729.3:p.Thr2858Ile
ENST00000382298.7:c.8573C>T	ENSP00000371735.3:p.Thr2858Ile
ENST00000402364.1:c.6323C>T	ENSP00000385844.1:p.Thr2108Ile
ENST00000423156.1:c.1058-5819C>T	ENSP00000390925.1:n.1058-5819C>T
ENST00000455470.5:c.2130-5819C>T
NM_001278055.1:c.8132C>T	NP_001264984.1:p.Thr2711Ile
NM_014363.5:c.8573C>T	NP_055178.3:p.Thr2858Ile
XM_005266338.1:c.8600C>T	XP_005266395.1:p.Thr2867Ile
XM_011535038.1:c.8624C>T	XP_011533340.1:p.Thr2875Ile
XM_011535039.1:c.8591C>T	XP_011533341.1:p.Thr2864Ile
XM_005266338.2:c.8600C>T	XP_005266395.1:p.Thr2867Ile
XM_011535039.2:c.8591C>T	XP_011533341.1:p.Thr2864Ile
XM_017020539.1:c.8564C>T	XP_016876028.1:p.Thr2855Ile
XM_024449337.1:c.8600C>T	XP_024305105.1:p.Thr2867Ile
NM_014363.6:c.8573C>T MANE Select	NP_055178.3:p.Thr2858Ile
NM_001278055.2:c.8132C>T	NP_001264984.1:p.Thr2711Ile