Canonical Allele Identifier: CA2575412488

Gene: SUCLA2

Linked Data

• gnomAD v4: 13-47988829-ATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988831_47988833del , CM000675.2:g.47988831_47988833del	GRCh38
NC_000013.10:g.48562966_48562968del , CM000675.1:g.48562966_48562968del	GRCh37
NC_000013.9:g.47460967_47460969del	NCBI36
NG_008241.1:g.17496_17498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.197+50_197+52del	ENSP00000495674.1:n.197+50_197+52del
ENST00000643023.1:c.371+50_371+52del	ENSP00000495664.1:n.371+50_371+52del
ENST00000643584.1:c.371+50_371+52del	ENSP00000494987.1:n.371+50_371+52del
ENST00000644338.1:c.371+50_371+52del	ENSP00000494723.1:n.371+50_371+52del
ENST00000646602.1:c.371+50_371+52del	ENSP00000495250.1:n.371+50_371+52del
ENST00000646804.1:c.197+50_197+52del	ENSP00000493977.1:n.197+50_197+52del
ENST00000646932.1:c.371+50_371+52del MANE Select	ENSP00000494360.1:n.371+50_371+52del
ENST00000647361.1:c.*164+50_*164+52del	ENSP00000494607.1:n.*164+50_*164+52del
ENST00000378654.8:c.371+50_371+52del	ENSP00000367923.3:n.371+50_371+52del
ENST00000433022.1:c.90+12348_90+12350del	ENSP00000415091.1:n.90+12348_90+12350del
ENST00000434484.5:c.161+50_161+52del	ENSP00000392771.1:n.161+50_161+52del
ENST00000470760.2:c.371+50_371+52del	ENSP00000488974.1:n.371+50_371+52del
ENST00000497202.6:c.465+50_465+52del	ENSP00000489175.1:n.465+50_465+52del
NM_003850.2:c.371+50_371+52del	NP_003841.1:n.371+50_371+52del
XM_011535292.1:c.134+50_134+52del	XP_011533594.1:n.134+50_134+52del
XM_011535293.1:c.-32+50_-32+52del	XP_011533595.1:n.-32+50_-32+52del
XR_941688.1:n.415+50_415+52del
NM_003850.3:c.371+50_371+52del MANE Select	NP_003841.1:n.371+50_371+52del