Canonical Allele Identifier: CA483555497

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48562676T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988541T>C , CM000675.2:g.47988541T>C	GRCh38
NC_000013.10:g.48562676T>C , CM000675.1:g.48562676T>C	GRCh37
NC_000013.9:g.47460677T>C	NCBI36
NG_008241.1:g.17787A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634878.2:c.8A>G
ENST00000642944.1:c.360A>G	ENSP00000495674.1:p.Gln120=
ENST00000643023.1:c.534A>G	ENSP00000495664.1:p.Gln178=
ENST00000643584.1:c.534A>G	ENSP00000494987.1:p.Gln178=
ENST00000644338.1:c.534A>G	ENSP00000494723.1:p.Gln178=
ENST00000646602.1:c.534A>G	ENSP00000495250.1:p.Gln178=
ENST00000646804.1:c.360A>G	ENSP00000493977.1:p.Gln120=
ENST00000646932.1:c.534A>G MANE Select	ENSP00000494360.1:p.Gln178=
ENST00000647361.1:c.*327A>G	ENSP00000494607.1:n.*327A>G
ENST00000378654.8:c.534A>G	ENSP00000367923.3:p.Gln178=
ENST00000433022.1:c.90+12639A>G	ENSP00000415091.1:n.90+12639A>G
ENST00000434484.5:c.324A>G	ENSP00000392771.1:p.Gln108=
ENST00000470760.2:c.534A>G	ENSP00000488974.1:p.Gln178=
ENST00000497202.6:c.628A>G	ENSP00000489175.1:n.628A>G
ENST00000634878.1:c.8A>G
NM_003850.2:c.534A>G	NP_003841.1:p.Gln178=
XM_011535292.1:c.297A>G	XP_011533594.1:p.Gln99=
XM_011535293.1:c.132A>G	XP_011533595.1:p.Gln44=
XR_941688.1:n.578A>G
NM_003850.3:c.534A>G MANE Select	NP_003841.1:p.Gln178=