Canonical Allele Identifier: CA387512949

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907907G>A (hg19) ; chr13:g.23333768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333768G>A , CM000675.2:g.23333768G>A	GRCh38
NC_000013.10:g.23907907G>A , CM000675.1:g.23907907G>A	GRCh37
NC_000013.9:g.22805907G>A	NCBI36
NG_012342.1:g.104935C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+20017C>T	ENSP00000508399.1:n.2185+20017C>T
ENST00000682944.1:c.10135C>T	ENSP00000507173.1:p.Gln3379Ter
ENST00000683210.1:c.2185+20017C>T	ENSP00000506739.1:n.2185+20017C>T
ENST00000683270.1:c.6445+3654C>T	ENSP00000507624.1:n.6445+3654C>T
ENST00000683367.1:c.2177-4284C>T	ENSP00000507780.1:n.2177-4284C>T
ENST00000683489.1:c.2292-3816C>T	ENSP00000508403.1:n.2292-3816C>T
ENST00000683680.1:c.2319-3816C>T	ENSP00000507223.1:n.2319-3816C>T
ENST00000684163.1:c.2204-4284C>T	ENSP00000508262.1:n.2204-4284C>T
ENST00000684196.1:n.4543-4284C>T
ENST00000684325.1:c.2186-12094C>T	ENSP00000508121.1:n.2186-12094C>T
ENST00000684385.1:c.2221-4284C>T	ENSP00000507855.1:n.2221-4284C>T
ENST00000684497.1:c.2186-11124C>T	ENSP00000507057.1:n.2186-11124C>T
ENST00000382292.9:c.10108C>T MANE Select	ENSP00000371729.3:p.Gln3370Ter
ENST00000423156.2:c.2186-4284C>T	ENSP00000390925.2:n.2186-4284C>T
ENST00000455470.6:c.2432-4284C>T	ENSP00000406565.2:n.2432-4284C>T
ENST00000382292.7:c.10108C>T	ENSP00000371729.3:p.Gln3370Ter
ENST00000382298.7:c.10108C>T	ENSP00000371735.3:p.Gln3370Ter
ENST00000402364.1:c.7858C>T	ENSP00000385844.1:p.Gln2620Ter
ENST00000423156.1:c.1058-4284C>T	ENSP00000390925.1:n.1058-4284C>T
ENST00000455470.5:c.2130-4284C>T
NM_001278055.1:c.9667C>T	NP_001264984.1:p.Gln3223Ter
NM_014363.5:c.10108C>T	NP_055178.3:p.Gln3370Ter
XM_005266338.1:c.10135C>T	XP_005266395.1:p.Gln3379Ter
XM_011535038.1:c.10159C>T	XP_011533340.1:p.Gln3387Ter
XM_011535039.1:c.10126C>T	XP_011533341.1:p.Gln3376Ter
XM_005266338.2:c.10135C>T	XP_005266395.1:p.Gln3379Ter
XM_011535039.2:c.10126C>T	XP_011533341.1:p.Gln3376Ter
XM_017020539.1:c.10099C>T	XP_016876028.1:p.Gln3367Ter
XM_024449337.1:c.10135C>T	XP_024305105.1:p.Gln3379Ter
NM_014363.6:c.10108C>T MANE Select	NP_055178.3:p.Gln3370Ter
NM_001278055.2:c.9667C>T	NP_001264984.1:p.Gln3223Ter