Canonical Allele Identifier: CA387515557

Gene: SACS

Linked Data

• gnomAD v4: 13-23334944-C-T
• COSMIC: COSM5842281 ; COSM5842282
• MyVariant Identifiers: chr13:g.23909083C>T (hg19) ; chr13:g.23334944C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334944C>T , CM000675.2:g.23334944C>T	GRCh38
NC_000013.10:g.23909083C>T , CM000675.1:g.23909083C>T	GRCh37
NC_000013.9:g.22807083C>T	NCBI36
NG_012342.1:g.103759G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18841G>A	ENSP00000508399.1:n.2185+18841G>A
ENST00000682944.1:c.8959G>A	ENSP00000507173.1:p.Val2987Met
ENST00000683210.1:c.2185+18841G>A	ENSP00000506739.1:n.2185+18841G>A
ENST00000683270.1:c.6445+2478G>A	ENSP00000507624.1:n.6445+2478G>A
ENST00000683367.1:c.2177-5460G>A	ENSP00000507780.1:n.2177-5460G>A
ENST00000683489.1:c.2292-4992G>A	ENSP00000508403.1:n.2292-4992G>A
ENST00000683680.1:c.2319-4992G>A	ENSP00000507223.1:n.2319-4992G>A
ENST00000684163.1:c.2204-5460G>A	ENSP00000508262.1:n.2204-5460G>A
ENST00000684196.1:n.4543-5460G>A
ENST00000684325.1:c.2186-13270G>A	ENSP00000508121.1:n.2186-13270G>A
ENST00000684385.1:c.2221-5460G>A	ENSP00000507855.1:n.2221-5460G>A
ENST00000684497.1:c.2186-12300G>A	ENSP00000507057.1:n.2186-12300G>A
ENST00000382292.9:c.8932G>A MANE Select	ENSP00000371729.3:p.Val2978Met
ENST00000423156.2:c.2186-5460G>A	ENSP00000390925.2:n.2186-5460G>A
ENST00000455470.6:c.2432-5460G>A	ENSP00000406565.2:n.2432-5460G>A
ENST00000382292.7:c.8932G>A	ENSP00000371729.3:p.Val2978Met
ENST00000382298.7:c.8932G>A	ENSP00000371735.3:p.Val2978Met
ENST00000402364.1:c.6682G>A	ENSP00000385844.1:p.Val2228Met
ENST00000423156.1:c.1058-5460G>A	ENSP00000390925.1:n.1058-5460G>A
ENST00000455470.5:c.2130-5460G>A
NM_001278055.1:c.8491G>A	NP_001264984.1:p.Val2831Met
NM_014363.5:c.8932G>A	NP_055178.3:p.Val2978Met
XM_005266338.1:c.8959G>A	XP_005266395.1:p.Val2987Met
XM_011535038.1:c.8983G>A	XP_011533340.1:p.Val2995Met
XM_011535039.1:c.8950G>A	XP_011533341.1:p.Val2984Met
XM_005266338.2:c.8959G>A	XP_005266395.1:p.Val2987Met
XM_011535039.2:c.8950G>A	XP_011533341.1:p.Val2984Met
XM_017020539.1:c.8923G>A	XP_016876028.1:p.Val2975Met
XM_024449337.1:c.8959G>A	XP_024305105.1:p.Val2987Met
NM_014363.6:c.8932G>A MANE Select	NP_055178.3:p.Val2978Met
NM_001278055.2:c.8491G>A	NP_001264984.1:p.Val2831Met