Canonical Allele Identifier: CA483708560

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48523634A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47949499A>C , CM000675.2:g.47949499A>C	GRCh38
NC_000013.10:g.48523634A>C , CM000675.1:g.48523634A>C	GRCh37
NC_000013.9:g.47421635A>C	NCBI36
NG_008241.1:g.56829T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634878.2:c.725T>G
ENST00000642944.1:c.1038T>G	ENSP00000495674.1:p.Val346=
ENST00000643023.1:c.1275T>G	ENSP00000495664.1:p.Val425=
ENST00000643584.1:c.1212T>G	ENSP00000494987.1:p.Val404=
ENST00000646804.1:c.1038T>G	ENSP00000493977.1:p.Val346=
ENST00000646932.1:c.1212T>G MANE Select	ENSP00000494360.1:p.Val404=
ENST00000647361.1:c.*1005T>G	ENSP00000494607.1:n.*1005T>G
ENST00000378654.8:c.1212T>G	ENSP00000367923.3:p.Val404=
ENST00000467222.1:n.520T>G
ENST00000493152.6:c.63T>G	ENSP00000489055.1:p.Val21=
ENST00000634878.1:c.725T>G
NM_003850.2:c.1212T>G	NP_003841.1:p.Val404=
XM_011535292.1:c.975T>G	XP_011533594.1:p.Val325=
XM_011535293.1:c.810T>G	XP_011533595.1:p.Val270=
NM_003850.3:c.1212T>G MANE Select	NP_003841.1:p.Val404=