Canonical Allele Identifier: CA2089813907
Gene: SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47988903C= , CM000675.2:g.47988903C= GRCh38
NC_000013.10:g.48563038C= , CM000675.1:g.48563038C= GRCh37
NC_000013.9:g.47461039C= NCBI36
NG_008241.1:g.17425G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642944.1:c.176G= ENSP00000495674.1:p.Gly59=
ENST00000643023.1:c.350G= ENSP00000495664.1:p.Gly117=
ENST00000643584.1:c.350G= ENSP00000494987.1:p.Gly117=
ENST00000644338.1:c.350G= ENSP00000494723.1:p.Gly117=
ENST00000646602.1:c.350G= ENSP00000495250.1:p.Gly117=
ENST00000646804.1:c.176G= ENSP00000493977.1:p.Gly59=
ENST00000646932.1:c.350G= MANE Select ENSP00000494360.1:p.Gly117=
ENST00000647361.1:c.*143G= ENSP00000494607.1:n.*143G=
ENST00000378654.8:c.350G= ENSP00000367923.3:p.Gly117=
ENST00000433022.1:c.90+12277G= ENSP00000415091.1:n.90+12277G=
ENST00000434484.5:c.140G= ENSP00000392771.1:p.Gly47=
ENST00000470760.2:c.350G= ENSP00000488974.1:p.Gly117=
ENST00000497202.6:c.444G= ENSP00000489175.1:n.444G=
NM_003850.2:c.350G= NP_003841.1:p.Gly117=
XM_011535292.1:c.113G= XP_011533594.1:p.Gly38=
XM_011535293.1:c.-53G= XP_011533595.1:n.-53G=
XR_941688.1:n.394G=
NM_003850.3:c.350G= MANE Select NP_003841.1:p.Gly117=