Canonical Allele Identifier: CA2089813901

Gene: SUCLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988892T= , CM000675.2:g.47988892T=	GRCh38
NC_000013.10:g.48563027T= , CM000675.1:g.48563027T=	GRCh37
NC_000013.9:g.47461028T=	NCBI36
NG_008241.1:g.17436A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.187A=	ENSP00000495674.1:p.Ile63=
ENST00000643023.1:c.361A=	ENSP00000495664.1:p.Ile121=
ENST00000643584.1:c.361A=	ENSP00000494987.1:p.Ile121=
ENST00000644338.1:c.361A=	ENSP00000494723.1:p.Ile121=
ENST00000646602.1:c.361A=	ENSP00000495250.1:p.Ile121=
ENST00000646804.1:c.187A=	ENSP00000493977.1:p.Ile63=
ENST00000646932.1:c.361A= MANE Select	ENSP00000494360.1:p.Ile121=
ENST00000647361.1:c.*154A=	ENSP00000494607.1:n.*154A=
ENST00000378654.8:c.361A=	ENSP00000367923.3:p.Ile121=
ENST00000433022.1:c.90+12288A=	ENSP00000415091.1:n.90+12288A=
ENST00000434484.5:c.151A=	ENSP00000392771.1:p.Ile51=
ENST00000470760.2:c.361A=	ENSP00000488974.1:p.Ile121=
ENST00000497202.6:c.455A=	ENSP00000489175.1:n.455A=
NM_003850.2:c.361A=	NP_003841.1:p.Ile121=
XM_011535292.1:c.124A=	XP_011533594.1:p.Ile42=
XM_011535293.1:c.-42A=	XP_011533595.1:n.-42A=
XR_941688.1:n.405A=
NM_003850.3:c.361A= MANE Select	NP_003841.1:p.Ile121=