Canonical Allele Identifier: CA387518874

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23910502C>T (hg19) ; chr13:g.23336363C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336363C>T , CM000675.2:g.23336363C>T	GRCh38
NC_000013.10:g.23910502C>T , CM000675.1:g.23910502C>T	GRCh37
NC_000013.9:g.22808502C>T	NCBI36
NG_012342.1:g.102340G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+17422G>A	ENSP00000508399.1:n.2185+17422G>A
ENST00000682944.1:c.7540G>A	ENSP00000507173.1:p.Ala2514Thr
ENST00000683210.1:c.2185+17422G>A	ENSP00000506739.1:n.2185+17422G>A
ENST00000683270.1:c.6445+1059G>A	ENSP00000507624.1:n.6445+1059G>A
ENST00000683367.1:c.2177-6879G>A	ENSP00000507780.1:n.2177-6879G>A
ENST00000683489.1:c.2291+5222G>A	ENSP00000508403.1:n.2291+5222G>A
ENST00000683680.1:c.2318+5222G>A	ENSP00000507223.1:n.2318+5222G>A
ENST00000684163.1:c.2204-6879G>A	ENSP00000508262.1:n.2204-6879G>A
ENST00000684196.1:n.4543-6879G>A
ENST00000684325.1:c.2186-14689G>A	ENSP00000508121.1:n.2186-14689G>A
ENST00000684385.1:c.2221-6879G>A	ENSP00000507855.1:n.2221-6879G>A
ENST00000684497.1:c.2186-13719G>A	ENSP00000507057.1:n.2186-13719G>A
ENST00000382292.9:c.7513G>A MANE Select	ENSP00000371729.3:p.Ala2505Thr
ENST00000423156.2:c.2186-6879G>A	ENSP00000390925.2:n.2186-6879G>A
ENST00000455470.6:c.2431+5082G>A	ENSP00000406565.2:n.2431+5082G>A
ENST00000382292.7:c.7513G>A	ENSP00000371729.3:p.Ala2505Thr
ENST00000382298.7:c.7513G>A	ENSP00000371735.3:p.Ala2505Thr
ENST00000402364.1:c.5263G>A	ENSP00000385844.1:p.Ala1755Thr
ENST00000423156.1:c.1058-6879G>A	ENSP00000390925.1:n.1058-6879G>A
ENST00000455470.5:c.2129+5082G>A
NM_001278055.1:c.7072G>A	NP_001264984.1:p.Ala2358Thr
NM_014363.5:c.7513G>A	NP_055178.3:p.Ala2505Thr
XM_005266338.1:c.7540G>A	XP_005266395.1:p.Ala2514Thr
XM_011535038.1:c.7564G>A	XP_011533340.1:p.Ala2522Thr
XM_011535039.1:c.7531G>A	XP_011533341.1:p.Ala2511Thr
XM_005266338.2:c.7540G>A	XP_005266395.1:p.Ala2514Thr
XM_011535039.2:c.7531G>A	XP_011533341.1:p.Ala2511Thr
XM_017020539.1:c.7504G>A	XP_016876028.1:p.Ala2502Thr
XM_024449337.1:c.7540G>A	XP_024305105.1:p.Ala2514Thr
NM_014363.6:c.7513G>A MANE Select	NP_055178.3:p.Ala2505Thr
NM_001278055.2:c.7072G>A	NP_001264984.1:p.Ala2358Thr