Canonical Allele Identifier: CA919266402
Gene: SUCLA2 HGNC NCBI

Linked Data

dbSNP Id: rs1593500762

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.47989081_47989085del , CM000675.2:g.47989081_47989085del GRCh38
NC_000013.10:g.48563216_48563220del , CM000675.1:g.48563216_48563220del GRCh37
NC_000013.9:g.47461217_47461221del NCBI36
NG_008241.1:g.17245_17249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642944.1:c.98-102_98-98del ENSP00000495674.1:n.98-102_98-98del
ENST00000643023.1:c.272-102_272-98del ENSP00000495664.1:n.272-102_272-98del
ENST00000643584.1:c.272-102_272-98del ENSP00000494987.1:n.272-102_272-98del
ENST00000644338.1:c.272-102_272-98del ENSP00000494723.1:n.272-102_272-98del
ENST00000646602.1:c.272-102_272-98del ENSP00000495250.1:n.272-102_272-98del
ENST00000646804.1:c.98-102_98-98del ENSP00000493977.1:n.98-102_98-98del
ENST00000646932.1:c.272-102_272-98del MANE Select ENSP00000494360.1:n.272-102_272-98del
ENST00000647361.1:c.*65-102_*65-98del ENSP00000494607.1:n.*65-102_*65-98del
ENST00000378654.8:c.272-102_272-98del ENSP00000367923.3:n.272-102_272-98del
ENST00000433022.1:c.90+12097_90+12101del ENSP00000415091.1:n.90+12097_90+12101del
ENST00000434484.5:c.62-102_62-98del ENSP00000392771.1:n.62-102_62-98del
ENST00000470760.2:c.272-102_272-98del ENSP00000488974.1:n.272-102_272-98del
ENST00000497202.6:c.366-102_366-98del ENSP00000489175.1:n.366-102_366-98del
NM_003850.2:c.272-102_272-98del NP_003841.1:n.272-102_272-98del
XM_011535292.1:c.35-102_35-98del XP_011533594.1:n.35-102_35-98del
XM_011535293.1:c.-131-102_-131-98del XP_011533595.1:n.-131-102_-131-98del
XR_941688.1:n.316-102_316-98del
NM_003850.3:c.272-102_272-98del MANE Select NP_003841.1:n.272-102_272-98del