Canonical Allele Identifier: CA387506241

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23905018A>C (hg19) ; chr13:g.23330879A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330879A>C , CM000675.2:g.23330879A>C	GRCh38
NC_000013.10:g.23905018A>C , CM000675.1:g.23905018A>C	GRCh37
NC_000013.9:g.22803018A>C	NCBI36
NG_012342.1:g.107824T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-18764T>G	ENSP00000508399.1:n.2186-18764T>G
ENST00000682944.1:c.13024T>G	ENSP00000507173.1:p.Tyr4342Asp
ENST00000683210.1:c.2185+22906T>G	ENSP00000506739.1:n.2185+22906T>G
ENST00000683270.1:c.6446-1395T>G	ENSP00000507624.1:n.6446-1395T>G
ENST00000683367.1:c.2177-1395T>G	ENSP00000507780.1:n.2177-1395T>G
ENST00000683489.1:c.2292-927T>G	ENSP00000508403.1:n.2292-927T>G
ENST00000683680.1:c.2319-927T>G	ENSP00000507223.1:n.2319-927T>G
ENST00000684163.1:c.2204-1395T>G	ENSP00000508262.1:n.2204-1395T>G
ENST00000684196.1:n.4543-1395T>G
ENST00000684325.1:c.2186-9205T>G	ENSP00000508121.1:n.2186-9205T>G
ENST00000684385.1:c.2221-1395T>G	ENSP00000507855.1:n.2221-1395T>G
ENST00000684497.1:c.2186-8235T>G	ENSP00000507057.1:n.2186-8235T>G
ENST00000382292.9:c.12997T>G MANE Select	ENSP00000371729.3:p.Tyr4333Asp
ENST00000423156.2:c.2186-1395T>G	ENSP00000390925.2:n.2186-1395T>G
ENST00000455470.6:c.2432-1395T>G	ENSP00000406565.2:n.2432-1395T>G
ENST00000382292.7:c.12997T>G	ENSP00000371729.3:p.Tyr4333Asp
ENST00000382298.7:c.12997T>G	ENSP00000371735.3:p.Tyr4333Asp
ENST00000402364.1:c.10747T>G	ENSP00000385844.1:p.Tyr3583Asp
ENST00000423156.1:c.1058-1395T>G	ENSP00000390925.1:n.1058-1395T>G
ENST00000455470.5:c.2130-1395T>G
NM_001278055.1:c.12556T>G	NP_001264984.1:p.Tyr4186Asp
NM_014363.5:c.12997T>G	NP_055178.3:p.Tyr4333Asp
XM_005266338.1:c.13024T>G	XP_005266395.1:p.Tyr4342Asp
XM_011535038.1:c.13048T>G	XP_011533340.1:p.Tyr4350Asp
XM_011535039.1:c.13015T>G	XP_011533341.1:p.Tyr4339Asp
XM_005266338.2:c.13024T>G	XP_005266395.1:p.Tyr4342Asp
XM_011535039.2:c.13015T>G	XP_011533341.1:p.Tyr4339Asp
XM_017020539.1:c.12988T>G	XP_016876028.1:p.Tyr4330Asp
XM_024449337.1:c.13024T>G	XP_024305105.1:p.Tyr4342Asp
NM_014363.6:c.12997T>G MANE Select	NP_055178.3:p.Tyr4333Asp
NM_001278055.2:c.12556T>G	NP_001264984.1:p.Tyr4186Asp