Canonical Allele Identifier: CA387505880

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23904858C>G (hg19) ; chr13:g.23330719C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330719C>G , CM000675.2:g.23330719C>G	GRCh38
NC_000013.10:g.23904858C>G , CM000675.1:g.23904858C>G	GRCh37
NC_000013.9:g.22802858C>G	NCBI36
NG_012342.1:g.107984G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18604G>C	ENSP00000508399.1:n.2186-18604G>C
ENST00000682944.1:c.13184G>C	ENSP00000507173.1:p.Arg4395Pro
ENST00000683210.1:c.2185+23066G>C	ENSP00000506739.1:n.2185+23066G>C
ENST00000683270.1:c.6446-1235G>C	ENSP00000507624.1:n.6446-1235G>C
ENST00000683367.1:c.2177-1235G>C	ENSP00000507780.1:n.2177-1235G>C
ENST00000683489.1:c.2292-767G>C	ENSP00000508403.1:n.2292-767G>C
ENST00000683680.1:c.2319-767G>C	ENSP00000507223.1:n.2319-767G>C
ENST00000684163.1:c.2204-1235G>C	ENSP00000508262.1:n.2204-1235G>C
ENST00000684196.1:n.4543-1235G>C
ENST00000684325.1:c.2186-9045G>C	ENSP00000508121.1:n.2186-9045G>C
ENST00000684385.1:c.2221-1235G>C	ENSP00000507855.1:n.2221-1235G>C
ENST00000684497.1:c.2186-8075G>C	ENSP00000507057.1:n.2186-8075G>C
ENST00000382292.9:c.13157G>C MANE Select	ENSP00000371729.3:p.Arg4386Pro
ENST00000423156.2:c.2186-1235G>C	ENSP00000390925.2:n.2186-1235G>C
ENST00000455470.6:c.2432-1235G>C	ENSP00000406565.2:n.2432-1235G>C
ENST00000382292.7:c.13157G>C	ENSP00000371729.3:p.Arg4386Pro
ENST00000382298.7:c.13157G>C	ENSP00000371735.3:p.Arg4386Pro
ENST00000402364.1:c.10907G>C	ENSP00000385844.1:p.Arg3636Pro
ENST00000423156.1:c.1058-1235G>C	ENSP00000390925.1:n.1058-1235G>C
ENST00000455470.5:c.2130-1235G>C
NM_001278055.1:c.12716G>C	NP_001264984.1:p.Arg4239Pro
NM_014363.5:c.13157G>C	NP_055178.3:p.Arg4386Pro
XM_005266338.1:c.13184G>C	XP_005266395.1:p.Arg4395Pro
XM_011535038.1:c.13208G>C	XP_011533340.1:p.Arg4403Pro
XM_011535039.1:c.13175G>C	XP_011533341.1:p.Arg4392Pro
XM_005266338.2:c.13184G>C	XP_005266395.1:p.Arg4395Pro
XM_011535039.2:c.13175G>C	XP_011533341.1:p.Arg4392Pro
XM_017020539.1:c.13148G>C	XP_016876028.1:p.Arg4383Pro
XM_024449337.1:c.13184G>C	XP_024305105.1:p.Arg4395Pro
NM_014363.6:c.13157G>C MANE Select	NP_055178.3:p.Arg4386Pro
NM_001278055.2:c.12716G>C	NP_001264984.1:p.Arg4239Pro