Canonical Allele Identifier: CA387527820

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23913259T>C (hg19) ; chr13:g.23339120T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23339120T>C , CM000675.2:g.23339120T>C	GRCh38
NC_000013.10:g.23913259T>C , CM000675.1:g.23913259T>C	GRCh37
NC_000013.9:g.22811259T>C	NCBI36
NG_012342.1:g.99583A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+14665A>G	ENSP00000508399.1:n.2185+14665A>G
ENST00000682944.1:c.4783A>G	ENSP00000507173.1:p.Asn1595Asp
ENST00000683210.1:c.2185+14665A>G	ENSP00000506739.1:n.2185+14665A>G
ENST00000683270.1:c.4747A>G	ENSP00000507624.1:p.Asn1583Asp
ENST00000683367.1:c.2177-9636A>G	ENSP00000507780.1:n.2177-9636A>G
ENST00000683489.1:c.2291+2465A>G	ENSP00000508403.1:n.2291+2465A>G
ENST00000683680.1:c.2318+2465A>G	ENSP00000507223.1:n.2318+2465A>G
ENST00000684163.1:c.2203+7691A>G	ENSP00000508262.1:n.2203+7691A>G
ENST00000684196.1:n.4543-9636A>G
ENST00000684325.1:c.2185+14665A>G	ENSP00000508121.1:n.2185+14665A>G
ENST00000684385.1:c.2220+7691A>G	ENSP00000507855.1:n.2220+7691A>G
ENST00000684497.1:c.2185+14665A>G	ENSP00000507057.1:n.2185+14665A>G
ENST00000382292.9:c.4756A>G MANE Select	ENSP00000371729.3:p.Asn1586Asp
ENST00000423156.2:c.2186-9636A>G	ENSP00000390925.2:n.2186-9636A>G
ENST00000455470.6:c.2431+2325A>G	ENSP00000406565.2:n.2431+2325A>G
ENST00000382292.7:c.4756A>G	ENSP00000371729.3:p.Asn1586Asp
ENST00000382298.7:c.4756A>G	ENSP00000371735.3:p.Asn1586Asp
ENST00000402364.1:c.2506A>G	ENSP00000385844.1:p.Asn836Asp
ENST00000423156.1:c.1058-9636A>G	ENSP00000390925.1:n.1058-9636A>G
ENST00000455470.5:c.2129+2325A>G
NM_001278055.1:c.4315A>G	NP_001264984.1:p.Asn1439Asp
NM_014363.5:c.4756A>G	NP_055178.3:p.Asn1586Asp
XM_005266338.1:c.4783A>G	XP_005266395.1:p.Asn1595Asp
XM_011535038.1:c.4807A>G	XP_011533340.1:p.Asn1603Asp
XM_011535039.1:c.4774A>G	XP_011533341.1:p.Asn1592Asp
XM_005266338.2:c.4783A>G	XP_005266395.1:p.Asn1595Asp
XM_011535039.2:c.4774A>G	XP_011533341.1:p.Asn1592Asp
XM_017020539.1:c.4747A>G	XP_016876028.1:p.Asn1583Asp
XM_024449337.1:c.4783A>G	XP_024305105.1:p.Asn1595Asp
NM_014363.6:c.4756A>G MANE Select	NP_055178.3:p.Asn1586Asp
NM_001278055.2:c.4315A>G	NP_001264984.1:p.Asn1439Asp