Canonical Allele Identifier: CA388151399

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48563048C>T (hg19) ; chr13:g.47988913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988913C>T , CM000675.2:g.47988913C>T	GRCh38
NC_000013.10:g.48563048C>T , CM000675.1:g.48563048C>T	GRCh37
NC_000013.9:g.47461049C>T	NCBI36
NG_008241.1:g.17415G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642944.1:c.166G>A	ENSP00000495674.1:p.Gly56Ser
ENST00000643023.1:c.340G>A	ENSP00000495664.1:p.Gly114Ser
ENST00000643584.1:c.340G>A	ENSP00000494987.1:p.Gly114Ser
ENST00000644338.1:c.340G>A	ENSP00000494723.1:p.Gly114Ser
ENST00000646602.1:c.340G>A	ENSP00000495250.1:p.Gly114Ser
ENST00000646804.1:c.166G>A	ENSP00000493977.1:p.Gly56Ser
ENST00000646932.1:c.340G>A MANE Select	ENSP00000494360.1:p.Gly114Ser
ENST00000647361.1:c.*133G>A	ENSP00000494607.1:n.*133G>A
ENST00000378654.8:c.340G>A	ENSP00000367923.3:p.Gly114Ser
ENST00000433022.1:c.90+12267G>A	ENSP00000415091.1:n.90+12267G>A
ENST00000434484.5:c.130G>A	ENSP00000392771.1:p.Gly44Ser
ENST00000470760.2:c.340G>A	ENSP00000488974.1:p.Gly114Ser
ENST00000497202.6:c.434G>A	ENSP00000489175.1:n.434G>A
NM_003850.2:c.340G>A	NP_003841.1:p.Gly114Ser
XM_011535292.1:c.103G>A	XP_011533594.1:p.Gly35Ser
XM_011535293.1:c.-63G>A	XP_011533595.1:n.-63G>A
XR_941688.1:n.384G>A
NM_003850.3:c.340G>A MANE Select	NP_003841.1:p.Gly114Ser