Canonical Allele Identifier: CA2089790489

Gene: SUCLA2

Linked Data

• dbSNP Id: rs1949759256
• gnomAD v4: 13-47949401-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47949403_47949404del , CM000675.2:g.47949403_47949404del	GRCh38
NC_000013.10:g.48523538_48523539del , CM000675.1:g.48523538_48523539del	GRCh37
NC_000013.9:g.47421539_47421540del	NCBI36
NG_008241.1:g.56925_56926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634878.2:c.741+80_741+81del
ENST00000642944.1:c.1054+80_1054+81del	ENSP00000495674.1:n.1054+80_1054+81del
ENST00000643023.1:c.1291+80_1291+81del	ENSP00000495664.1:n.1291+80_1291+81del
ENST00000643584.1:c.1228+80_1228+81del	ENSP00000494987.1:n.1228+80_1228+81del
ENST00000646804.1:c.1054+80_1054+81del	ENSP00000493977.1:n.1054+80_1054+81del
ENST00000646932.1:c.1228+80_1228+81del MANE Select	ENSP00000494360.1:n.1228+80_1228+81del
ENST00000647361.1:c.*1021+80_*1021+81del	ENSP00000494607.1:n.*1021+80_*1021+81del
ENST00000378654.8:c.1228+80_1228+81del	ENSP00000367923.3:n.1228+80_1228+81del
ENST00000467222.1:n.536+80_536+81del
ENST00000493152.6:c.79+80_79+81del	ENSP00000489055.1:n.79+80_79+81del
ENST00000634878.1:c.741+80_741+81del
NM_003850.2:c.1228+80_1228+81del	NP_003841.1:n.1228+80_1228+81del
XM_011535292.1:c.991+80_991+81del	XP_011533594.1:n.991+80_991+81del
XM_011535293.1:c.826+80_826+81del	XP_011533595.1:n.826+80_826+81del
NM_003850.3:c.1228+80_1228+81del MANE Select	NP_003841.1:n.1228+80_1228+81del