Canonical Allele Identifier: CA2089813816

Gene: SUCLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988688T= , CM000675.2:g.47988688T=	GRCh38
NC_000013.10:g.48562823T= , CM000675.1:g.48562823T=	GRCh37
NC_000013.9:g.47460824T=	NCBI36
NG_008241.1:g.17640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.213A=	ENSP00000495674.1:p.Lys71=
ENST00000643023.1:c.387A=	ENSP00000495664.1:p.Lys129=
ENST00000643584.1:c.387A=	ENSP00000494987.1:p.Lys129=
ENST00000644338.1:c.387A=	ENSP00000494723.1:p.Lys129=
ENST00000646602.1:c.387A=	ENSP00000495250.1:p.Lys129=
ENST00000646804.1:c.213A=	ENSP00000493977.1:p.Lys71=
ENST00000646932.1:c.387A= MANE Select	ENSP00000494360.1:p.Lys129=
ENST00000647361.1:c.*180A=	ENSP00000494607.1:n.*180A=
ENST00000378654.8:c.387A=	ENSP00000367923.3:p.Lys129=
ENST00000433022.1:c.90+12492A=	ENSP00000415091.1:n.90+12492A=
ENST00000434484.5:c.177A=	ENSP00000392771.1:p.Lys59=
ENST00000470760.2:c.387A=	ENSP00000488974.1:p.Lys129=
ENST00000497202.6:c.481A=	ENSP00000489175.1:n.481A=
NM_003850.2:c.387A=	NP_003841.1:p.Lys129=
XM_011535292.1:c.150A=	XP_011533594.1:p.Lys50=
XM_011535293.1:c.-16A=	XP_011533595.1:n.-16A=
XR_941688.1:n.431A=
NM_003850.3:c.387A= MANE Select	NP_003841.1:p.Lys129=