Canonical Allele Identifier: CA2089813831
Gene: SUCLA2 HGNC NCBI

Linked Data

dbSNP Id: rs1950125711

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47988731_47988732dup , CM000675.2:g.47988731_47988732dup GRCh38
NC_000013.10:g.48562866_48562867dup , CM000675.1:g.48562866_48562867dup GRCh37
NC_000013.9:g.47460867_47460868dup NCBI36
NG_008241.1:g.17599_17600dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642944.1:c.198-26_198-25dup ENSP00000495674.1:n.198-26_198-25dup
ENST00000643023.1:c.372-26_372-25dup ENSP00000495664.1:n.372-26_372-25dup
ENST00000643584.1:c.372-26_372-25dup ENSP00000494987.1:n.372-26_372-25dup
ENST00000644338.1:c.372-26_372-25dup ENSP00000494723.1:n.372-26_372-25dup
ENST00000646602.1:c.372-26_372-25dup ENSP00000495250.1:n.372-26_372-25dup
ENST00000646804.1:c.198-26_198-25dup ENSP00000493977.1:n.198-26_198-25dup
ENST00000646932.1:c.372-26_372-25dup MANE Select ENSP00000494360.1:n.372-26_372-25dup
ENST00000647361.1:c.*165-26_*165-25dup ENSP00000494607.1:n.*165-26_*165-25dup
ENST00000378654.8:c.372-26_372-25dup ENSP00000367923.3:n.372-26_372-25dup
ENST00000433022.1:c.90+12451_90+12452dup ENSP00000415091.1:n.90+12451_90+12452dup
ENST00000434484.5:c.162-26_162-25dup ENSP00000392771.1:n.162-26_162-25dup
ENST00000470760.2:c.372-26_372-25dup ENSP00000488974.1:n.372-26_372-25dup
ENST00000497202.6:c.466-26_466-25dup ENSP00000489175.1:n.466-26_466-25dup
NM_003850.2:c.372-26_372-25dup NP_003841.1:n.372-26_372-25dup
XM_011535292.1:c.135-26_135-25dup XP_011533594.1:n.135-26_135-25dup
XM_011535293.1:c.-31-26_-31-25dup XP_011533595.1:n.-31-26_-31-25dup
XR_941688.1:n.416-26_416-25dup
NM_003850.3:c.372-26_372-25dup MANE Select NP_003841.1:n.372-26_372-25dup