Canonical Allele Identifier: CA2089790526
Gene: SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47949491C= , CM000675.2:g.47949491C= GRCh38
NC_000013.10:g.48523626C= , CM000675.1:g.48523626C= GRCh37
NC_000013.9:g.47421627C= NCBI36
NG_008241.1:g.56837G=

Transcript Alleles

HGVS Amino-acid change
ENST00000634878.2:c.733G=
ENST00000642944.1:c.1046G= ENSP00000495674.1:p.Arg349=
ENST00000643023.1:c.1283G= ENSP00000495664.1:p.Arg428=
ENST00000643584.1:c.1220G= ENSP00000494987.1:p.Arg407=
ENST00000646804.1:c.1046G= ENSP00000493977.1:p.Arg349=
ENST00000646932.1:c.1220G= MANE Select ENSP00000494360.1:p.Arg407=
ENST00000647361.1:c.*1013G= ENSP00000494607.1:n.*1013G=
ENST00000378654.8:c.1220G= ENSP00000367923.3:p.Arg407=
ENST00000467222.1:n.528G=
ENST00000493152.6:c.71G= ENSP00000489055.1:p.Arg24=
ENST00000634878.1:c.733G=
NM_003850.2:c.1220G= NP_003841.1:p.Arg407=
XM_011535292.1:c.983G= XP_011533594.1:p.Arg328=
XM_011535293.1:c.818G= XP_011533595.1:p.Arg273=
NM_003850.3:c.1220G= MANE Select NP_003841.1:p.Arg407=