Canonical Allele Identifier: CA2622965598

Gene: SUCLA2

Linked Data

• gnomAD v4: 13-47988842-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988845del , CM000675.2:g.47988845del	GRCh38
NC_000013.10:g.48562980del , CM000675.1:g.48562980del	GRCh37
NC_000013.9:g.47460981del	NCBI36
NG_008241.1:g.17485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.197+39del	ENSP00000495674.1:n.197+39del
ENST00000643023.1:c.371+39del	ENSP00000495664.1:n.371+39del
ENST00000643584.1:c.371+39del	ENSP00000494987.1:n.371+39del
ENST00000644338.1:c.371+39del	ENSP00000494723.1:n.371+39del
ENST00000646602.1:c.371+39del	ENSP00000495250.1:n.371+39del
ENST00000646804.1:c.197+39del	ENSP00000493977.1:n.197+39del
ENST00000646932.1:c.371+39del MANE Select	ENSP00000494360.1:n.371+39del
ENST00000647361.1:c.*164+39del	ENSP00000494607.1:n.*164+39del
ENST00000378654.8:c.371+39del	ENSP00000367923.3:n.371+39del
ENST00000433022.1:c.90+12337del	ENSP00000415091.1:n.90+12337del
ENST00000434484.5:c.161+39del	ENSP00000392771.1:n.161+39del
ENST00000470760.2:c.371+39del	ENSP00000488974.1:n.371+39del
ENST00000497202.6:c.465+39del	ENSP00000489175.1:n.465+39del
NM_003850.2:c.371+39del	NP_003841.1:n.371+39del
XM_011535292.1:c.134+39del	XP_011533594.1:n.134+39del
XM_011535293.1:c.-32+39del	XP_011533595.1:n.-32+39del
XR_941688.1:n.415+39del
NM_003850.3:c.371+39del MANE Select	NP_003841.1:n.371+39del