Canonical Allele Identifier: CA2089790494

Gene: SUCLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47949426T= , CM000675.2:g.47949426T=	GRCh38
NC_000013.10:g.48523561T= , CM000675.1:g.48523561T=	GRCh37
NC_000013.9:g.47421562T=	NCBI36
NG_008241.1:g.56902A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634878.2:c.741+57A=
ENST00000642944.1:c.1054+57A=	ENSP00000495674.1:n.1054+57A=
ENST00000643023.1:c.1291+57A=	ENSP00000495664.1:n.1291+57A=
ENST00000643584.1:c.1228+57A=	ENSP00000494987.1:n.1228+57A=
ENST00000646804.1:c.1054+57A=	ENSP00000493977.1:n.1054+57A=
ENST00000646932.1:c.1228+57A= MANE Select	ENSP00000494360.1:n.1228+57A=
ENST00000647361.1:c.*1021+57A=	ENSP00000494607.1:n.*1021+57A=
ENST00000378654.8:c.1228+57A=	ENSP00000367923.3:n.1228+57A=
ENST00000467222.1:n.536+57A=
ENST00000493152.6:c.79+57A=	ENSP00000489055.1:n.79+57A=
ENST00000634878.1:c.741+57A=
NM_003850.2:c.1228+57A=	NP_003841.1:n.1228+57A=
XM_011535292.1:c.991+57A=	XP_011533594.1:n.991+57A=
XM_011535293.1:c.826+57A=	XP_011533595.1:n.826+57A=
NM_003850.3:c.1228+57A= MANE Select	NP_003841.1:n.1228+57A=