Canonical Allele Identifier: CA483708546

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48523631C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47949496C>T , CM000675.2:g.47949496C>T	GRCh38
NC_000013.10:g.48523631C>T , CM000675.1:g.48523631C>T	GRCh37
NC_000013.9:g.47421632C>T	NCBI36
NG_008241.1:g.56832G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000634878.2:c.728G>A
ENST00000642944.1:c.1041G>A	ENSP00000495674.1:p.Val347=
ENST00000643023.1:c.1278G>A	ENSP00000495664.1:p.Val426=
ENST00000643584.1:c.1215G>A	ENSP00000494987.1:p.Val405=
ENST00000646804.1:c.1041G>A	ENSP00000493977.1:p.Val347=
ENST00000646932.1:c.1215G>A MANE Select	ENSP00000494360.1:p.Val405=
ENST00000647361.1:c.*1008G>A	ENSP00000494607.1:n.*1008G>A
ENST00000378654.8:c.1215G>A	ENSP00000367923.3:p.Val405=
ENST00000467222.1:n.523G>A
ENST00000493152.6:c.66G>A	ENSP00000489055.1:p.Val22=
ENST00000634878.1:c.728G>A
NM_003850.2:c.1215G>A	NP_003841.1:p.Val405=
XM_011535292.1:c.978G>A	XP_011533594.1:p.Val326=
XM_011535293.1:c.813G>A	XP_011533595.1:p.Val271=
NM_003850.3:c.1215G>A MANE Select	NP_003841.1:p.Val405=