Canonical Allele Identifier: CA483555629

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48563076A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988941A>T , CM000675.2:g.47988941A>T	GRCh38
NC_000013.10:g.48563076A>T , CM000675.1:g.48563076A>T	GRCh37
NC_000013.9:g.47461077A>T	NCBI36
NG_008241.1:g.17387T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.138T>A	ENSP00000495674.1:p.Gly46=
ENST00000643023.1:c.312T>A	ENSP00000495664.1:p.Gly104=
ENST00000643584.1:c.312T>A	ENSP00000494987.1:p.Gly104=
ENST00000644338.1:c.312T>A	ENSP00000494723.1:p.Gly104=
ENST00000646602.1:c.312T>A	ENSP00000495250.1:p.Gly104=
ENST00000646804.1:c.138T>A	ENSP00000493977.1:p.Gly46=
ENST00000646932.1:c.312T>A MANE Select	ENSP00000494360.1:p.Gly104=
ENST00000647361.1:c.*105T>A	ENSP00000494607.1:n.*105T>A
ENST00000378654.8:c.312T>A	ENSP00000367923.3:p.Gly104=
ENST00000433022.1:c.90+12239T>A	ENSP00000415091.1:n.90+12239T>A
ENST00000434484.5:c.102T>A	ENSP00000392771.1:p.Gly34=
ENST00000470760.2:c.312T>A	ENSP00000488974.1:p.Gly104=
ENST00000497202.6:c.406T>A	ENSP00000489175.1:p.Trp136Arg
NM_003850.2:c.312T>A	NP_003841.1:p.Gly104=
XM_011535292.1:c.75T>A	XP_011533594.1:p.Gly25=
XM_011535293.1:c.-91T>A	XP_011533595.1:n.-91T>A
XR_941688.1:n.356T>A
NM_003850.3:c.312T>A MANE Select	NP_003841.1:p.Gly104=