Canonical Allele Identifier: CA388151031
Gene: SUCLA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47988690T>G , CM000675.2:g.47988690T>G GRCh38
NC_000013.10:g.48562825T>G , CM000675.1:g.48562825T>G GRCh37
NC_000013.9:g.47460826T>G NCBI36
NG_008241.1:g.17638A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642944.1:c.211A>C ENSP00000495674.1:p.Lys71Gln
ENST00000643023.1:c.385A>C ENSP00000495664.1:p.Lys129Gln
ENST00000643584.1:c.385A>C ENSP00000494987.1:p.Lys129Gln
ENST00000644338.1:c.385A>C ENSP00000494723.1:p.Lys129Gln
ENST00000646602.1:c.385A>C ENSP00000495250.1:p.Lys129Gln
ENST00000646804.1:c.211A>C ENSP00000493977.1:p.Lys71Gln
ENST00000646932.1:c.385A>C MANE Select ENSP00000494360.1:p.Lys129Gln
ENST00000647361.1:c.*178A>C ENSP00000494607.1:n.*178A>C
ENST00000378654.8:c.385A>C ENSP00000367923.3:p.Lys129Gln
ENST00000433022.1:c.90+12490A>C ENSP00000415091.1:n.90+12490A>C
ENST00000434484.5:c.175A>C ENSP00000392771.1:p.Lys59Gln
ENST00000470760.2:c.385A>C ENSP00000488974.1:p.Lys129Gln
ENST00000497202.6:c.479A>C ENSP00000489175.1:n.479A>C
NM_003850.2:c.385A>C NP_003841.1:p.Lys129Gln
XM_011535292.1:c.148A>C XP_011533594.1:p.Lys50Gln
XM_011535293.1:c.-18A>C XP_011533595.1:n.-18A>C
XR_941688.1:n.429A>C
NM_003850.3:c.385A>C MANE Select NP_003841.1:p.Lys129Gln