Canonical Allele Identifier: CA387506114

Gene: SACS

Linked Data

• gnomAD v4: 13-23330825-C-T
• MyVariant Identifiers: chr13:g.23904964C>T (hg19) ; chr13:g.23330825C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330825C>T , CM000675.2:g.23330825C>T	GRCh38
NC_000013.10:g.23904964C>T , CM000675.1:g.23904964C>T	GRCh37
NC_000013.9:g.22802964C>T	NCBI36
NG_012342.1:g.107878G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18710G>A	ENSP00000508399.1:n.2186-18710G>A
ENST00000682944.1:c.13078G>A	ENSP00000507173.1:p.Val4360Ile
ENST00000683210.1:c.2185+22960G>A	ENSP00000506739.1:n.2185+22960G>A
ENST00000683270.1:c.6446-1341G>A	ENSP00000507624.1:n.6446-1341G>A
ENST00000683367.1:c.2177-1341G>A	ENSP00000507780.1:n.2177-1341G>A
ENST00000683489.1:c.2292-873G>A	ENSP00000508403.1:n.2292-873G>A
ENST00000683680.1:c.2319-873G>A	ENSP00000507223.1:n.2319-873G>A
ENST00000684163.1:c.2204-1341G>A	ENSP00000508262.1:n.2204-1341G>A
ENST00000684196.1:n.4543-1341G>A
ENST00000684325.1:c.2186-9151G>A	ENSP00000508121.1:n.2186-9151G>A
ENST00000684385.1:c.2221-1341G>A	ENSP00000507855.1:n.2221-1341G>A
ENST00000684497.1:c.2186-8181G>A	ENSP00000507057.1:n.2186-8181G>A
ENST00000382292.9:c.13051G>A MANE Select	ENSP00000371729.3:p.Val4351Ile
ENST00000423156.2:c.2186-1341G>A	ENSP00000390925.2:n.2186-1341G>A
ENST00000455470.6:c.2432-1341G>A	ENSP00000406565.2:n.2432-1341G>A
ENST00000382292.7:c.13051G>A	ENSP00000371729.3:p.Val4351Ile
ENST00000382298.7:c.13051G>A	ENSP00000371735.3:p.Val4351Ile
ENST00000402364.1:c.10801G>A	ENSP00000385844.1:p.Val3601Ile
ENST00000423156.1:c.1058-1341G>A	ENSP00000390925.1:n.1058-1341G>A
ENST00000455470.5:c.2130-1341G>A
NM_001278055.1:c.12610G>A	NP_001264984.1:p.Val4204Ile
NM_014363.5:c.13051G>A	NP_055178.3:p.Val4351Ile
XM_005266338.1:c.13078G>A	XP_005266395.1:p.Val4360Ile
XM_011535038.1:c.13102G>A	XP_011533340.1:p.Val4368Ile
XM_011535039.1:c.13069G>A	XP_011533341.1:p.Val4357Ile
XM_005266338.2:c.13078G>A	XP_005266395.1:p.Val4360Ile
XM_011535039.2:c.13069G>A	XP_011533341.1:p.Val4357Ile
XM_017020539.1:c.13042G>A	XP_016876028.1:p.Val4348Ile
XM_024449337.1:c.13078G>A	XP_024305105.1:p.Val4360Ile
NM_014363.6:c.13051G>A MANE Select	NP_055178.3:p.Val4351Ile
NM_001278055.2:c.12610G>A	NP_001264984.1:p.Val4204Ile