Canonical Allele Identifier: CA388151531

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48563069C>A (hg19) ; chr13:g.47988934C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988934C>A , CM000675.2:g.47988934C>A	GRCh38
NC_000013.10:g.48563069C>A , CM000675.1:g.48563069C>A	GRCh37
NC_000013.9:g.47461070C>A	NCBI36
NG_008241.1:g.17394G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.145G>T	ENSP00000495674.1:p.Gly49Ter
ENST00000643023.1:c.319G>T	ENSP00000495664.1:p.Gly107Ter
ENST00000643584.1:c.319G>T	ENSP00000494987.1:p.Gly107Ter
ENST00000644338.1:c.319G>T	ENSP00000494723.1:p.Gly107Ter
ENST00000646602.1:c.319G>T	ENSP00000495250.1:p.Gly107Ter
ENST00000646804.1:c.145G>T	ENSP00000493977.1:p.Gly49Ter
ENST00000646932.1:c.319G>T MANE Select	ENSP00000494360.1:p.Gly107Ter
ENST00000647361.1:c.*112G>T	ENSP00000494607.1:n.*112G>T
ENST00000378654.8:c.319G>T	ENSP00000367923.3:p.Gly107Ter
ENST00000433022.1:c.90+12246G>T	ENSP00000415091.1:n.90+12246G>T
ENST00000434484.5:c.109G>T	ENSP00000392771.1:p.Gly37Ter
ENST00000470760.2:c.319G>T	ENSP00000488974.1:p.Gly107Ter
ENST00000497202.6:c.413G>T	ENSP00000489175.1:n.413G>T
NM_003850.2:c.319G>T	NP_003841.1:p.Gly107Ter
XM_011535292.1:c.82G>T	XP_011533594.1:p.Gly28Ter
XM_011535293.1:c.-84G>T	XP_011533595.1:n.-84G>T
XR_941688.1:n.363G>T
NM_003850.3:c.319G>T MANE Select	NP_003841.1:p.Gly107Ter