Canonical Allele Identifier: CA2089813909
Gene: SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47988911G= , CM000675.2:g.47988911G= GRCh38
NC_000013.10:g.48563046G= , CM000675.1:g.48563046G= GRCh37
NC_000013.9:g.47461047G= NCBI36
NG_008241.1:g.17417C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642944.1:c.168C= ENSP00000495674.1:p.Gly56=
ENST00000643023.1:c.342C= ENSP00000495664.1:p.Gly114=
ENST00000643584.1:c.342C= ENSP00000494987.1:p.Gly114=
ENST00000644338.1:c.342C= ENSP00000494723.1:p.Gly114=
ENST00000646602.1:c.342C= ENSP00000495250.1:p.Gly114=
ENST00000646804.1:c.168C= ENSP00000493977.1:p.Gly56=
ENST00000646932.1:c.342C= MANE Select ENSP00000494360.1:p.Gly114=
ENST00000647361.1:c.*135C= ENSP00000494607.1:n.*135C=
ENST00000378654.8:c.342C= ENSP00000367923.3:p.Gly114=
ENST00000433022.1:c.90+12269C= ENSP00000415091.1:n.90+12269C=
ENST00000434484.5:c.132C= ENSP00000392771.1:p.Gly44=
ENST00000470760.2:c.342C= ENSP00000488974.1:p.Gly114=
ENST00000497202.6:c.436C= ENSP00000489175.1:n.436C=
NM_003850.2:c.342C= NP_003841.1:p.Gly114=
XM_011535292.1:c.105C= XP_011533594.1:p.Gly35=
XM_011535293.1:c.-61C= XP_011533595.1:n.-61C=
XR_941688.1:n.386C=
NM_003850.3:c.342C= MANE Select NP_003841.1:p.Gly114=