Canonical Allele Identifier: CA387505684

Gene: SACS

Linked Data

• dbSNP Id: rs772374399
• MyVariant Identifiers: chr13:g.23904771T>G (hg19) ; chr13:g.23330632T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330632T>G , CM000675.2:g.23330632T>G	GRCh38
NC_000013.10:g.23904771T>G , CM000675.1:g.23904771T>G	GRCh37
NC_000013.9:g.22802771T>G	NCBI36
NG_012342.1:g.108071A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18517A>C	ENSP00000508399.1:n.2186-18517A>C
ENST00000682944.1:c.13271A>C	ENSP00000507173.1:p.Gln4424Pro
ENST00000683210.1:c.2185+23153A>C	ENSP00000506739.1:n.2185+23153A>C
ENST00000683270.1:c.6446-1148A>C	ENSP00000507624.1:n.6446-1148A>C
ENST00000683367.1:c.2177-1148A>C	ENSP00000507780.1:n.2177-1148A>C
ENST00000683489.1:c.2292-680A>C	ENSP00000508403.1:n.2292-680A>C
ENST00000683680.1:c.2319-680A>C	ENSP00000507223.1:n.2319-680A>C
ENST00000684163.1:c.2204-1148A>C	ENSP00000508262.1:n.2204-1148A>C
ENST00000684196.1:n.4543-1148A>C
ENST00000684325.1:c.2186-8958A>C	ENSP00000508121.1:n.2186-8958A>C
ENST00000684385.1:c.2221-1148A>C	ENSP00000507855.1:n.2221-1148A>C
ENST00000684497.1:c.2186-7988A>C	ENSP00000507057.1:n.2186-7988A>C
ENST00000382292.9:c.13244A>C MANE Select	ENSP00000371729.3:p.Gln4415Pro
ENST00000423156.2:c.2186-1148A>C	ENSP00000390925.2:n.2186-1148A>C
ENST00000455470.6:c.2432-1148A>C	ENSP00000406565.2:n.2432-1148A>C
ENST00000382292.7:c.13244A>C	ENSP00000371729.3:p.Gln4415Pro
ENST00000382298.7:c.13244A>C	ENSP00000371735.3:p.Gln4415Pro
ENST00000402364.1:c.10994A>C	ENSP00000385844.1:p.Gln3665Pro
ENST00000423156.1:c.1058-1148A>C	ENSP00000390925.1:n.1058-1148A>C
ENST00000455470.5:c.2130-1148A>C
NM_001278055.1:c.12803A>C	NP_001264984.1:p.Gln4268Pro
NM_014363.5:c.13244A>C	NP_055178.3:p.Gln4415Pro
XM_005266338.1:c.13271A>C	XP_005266395.1:p.Gln4424Pro
XM_011535038.1:c.13295A>C	XP_011533340.1:p.Gln4432Pro
XM_011535039.1:c.13262A>C	XP_011533341.1:p.Gln4421Pro
XM_005266338.2:c.13271A>C	XP_005266395.1:p.Gln4424Pro
XM_011535039.2:c.13262A>C	XP_011533341.1:p.Gln4421Pro
XM_017020539.1:c.13235A>C	XP_016876028.1:p.Gln4412Pro
XM_024449337.1:c.13271A>C	XP_024305105.1:p.Gln4424Pro
NM_014363.6:c.13244A>C MANE Select	NP_055178.3:p.Gln4415Pro
NM_001278055.2:c.12803A>C	NP_001264984.1:p.Gln4268Pro