Canonical Allele Identifier: CA387515592

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909098C>T (hg19) ; chr13:g.23334959C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334959C>T , CM000675.2:g.23334959C>T	GRCh38
NC_000013.10:g.23909098C>T , CM000675.1:g.23909098C>T	GRCh37
NC_000013.9:g.22807098C>T	NCBI36
NG_012342.1:g.103744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18826G>A	ENSP00000508399.1:n.2185+18826G>A
ENST00000682944.1:c.8944G>A	ENSP00000507173.1:p.Asp2982Asn
ENST00000683210.1:c.2185+18826G>A	ENSP00000506739.1:n.2185+18826G>A
ENST00000683270.1:c.6445+2463G>A	ENSP00000507624.1:n.6445+2463G>A
ENST00000683367.1:c.2177-5475G>A	ENSP00000507780.1:n.2177-5475G>A
ENST00000683489.1:c.2292-5007G>A	ENSP00000508403.1:n.2292-5007G>A
ENST00000683680.1:c.2319-5007G>A	ENSP00000507223.1:n.2319-5007G>A
ENST00000684163.1:c.2204-5475G>A	ENSP00000508262.1:n.2204-5475G>A
ENST00000684196.1:n.4543-5475G>A
ENST00000684325.1:c.2186-13285G>A	ENSP00000508121.1:n.2186-13285G>A
ENST00000684385.1:c.2221-5475G>A	ENSP00000507855.1:n.2221-5475G>A
ENST00000684497.1:c.2186-12315G>A	ENSP00000507057.1:n.2186-12315G>A
ENST00000382292.9:c.8917G>A MANE Select	ENSP00000371729.3:p.Asp2973Asn
ENST00000423156.2:c.2186-5475G>A	ENSP00000390925.2:n.2186-5475G>A
ENST00000455470.6:c.2432-5475G>A	ENSP00000406565.2:n.2432-5475G>A
ENST00000382292.7:c.8917G>A	ENSP00000371729.3:p.Asp2973Asn
ENST00000382298.7:c.8917G>A	ENSP00000371735.3:p.Asp2973Asn
ENST00000402364.1:c.6667G>A	ENSP00000385844.1:p.Asp2223Asn
ENST00000423156.1:c.1058-5475G>A	ENSP00000390925.1:n.1058-5475G>A
ENST00000455470.5:c.2130-5475G>A
NM_001278055.1:c.8476G>A	NP_001264984.1:p.Asp2826Asn
NM_014363.5:c.8917G>A	NP_055178.3:p.Asp2973Asn
XM_005266338.1:c.8944G>A	XP_005266395.1:p.Asp2982Asn
XM_011535038.1:c.8968G>A	XP_011533340.1:p.Asp2990Asn
XM_011535039.1:c.8935G>A	XP_011533341.1:p.Asp2979Asn
XM_005266338.2:c.8944G>A	XP_005266395.1:p.Asp2982Asn
XM_011535039.2:c.8935G>A	XP_011533341.1:p.Asp2979Asn
XM_017020539.1:c.8908G>A	XP_016876028.1:p.Asp2970Asn
XM_024449337.1:c.8944G>A	XP_024305105.1:p.Asp2982Asn
NM_014363.6:c.8917G>A MANE Select	NP_055178.3:p.Asp2973Asn
NM_001278055.2:c.8476G>A	NP_001264984.1:p.Asp2826Asn