Canonical Allele Identifier: CA2089813898

Gene: SUCLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988889C= , CM000675.2:g.47988889C=	GRCh38
NC_000013.10:g.48563024C= , CM000675.1:g.48563024C=	GRCh37
NC_000013.9:g.47461025C=	NCBI36
NG_008241.1:g.17439G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.190G=	ENSP00000495674.1:p.Val64=
ENST00000643023.1:c.364G=	ENSP00000495664.1:p.Val122=
ENST00000643584.1:c.364G=	ENSP00000494987.1:p.Val122=
ENST00000644338.1:c.364G=	ENSP00000494723.1:p.Val122=
ENST00000646602.1:c.364G=	ENSP00000495250.1:p.Val122=
ENST00000646804.1:c.190G=	ENSP00000493977.1:p.Val64=
ENST00000646932.1:c.364G= MANE Select	ENSP00000494360.1:p.Val122=
ENST00000647361.1:c.*157G=	ENSP00000494607.1:n.*157G=
ENST00000378654.8:c.364G=	ENSP00000367923.3:p.Val122=
ENST00000433022.1:c.90+12291G=	ENSP00000415091.1:n.90+12291G=
ENST00000434484.5:c.154G=	ENSP00000392771.1:p.Val52=
ENST00000470760.2:c.364G=	ENSP00000488974.1:p.Val122=
ENST00000497202.6:c.458G=	ENSP00000489175.1:n.458G=
NM_003850.2:c.364G=	NP_003841.1:p.Val122=
XM_011535292.1:c.127G=	XP_011533594.1:p.Val43=
XM_011535293.1:c.-39G=	XP_011533595.1:n.-39G=
XR_941688.1:n.408G=
NM_003850.3:c.364G= MANE Select	NP_003841.1:p.Val122=