Canonical Allele Identifier: CA483555588

Gene: SUCLA2

Linked Data

• dbSNP Id: rs1218701299
• MyVariant Identifiers: chr13:g.48562845del (hg19) ; chr13:g.47988710del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988710del , CM000675.2:g.47988710del	GRCh38
NC_000013.10:g.48562845del , CM000675.1:g.48562845del	GRCh37
NC_000013.9:g.47460846del	NCBI36
NG_008241.1:g.17618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.198-7del	ENSP00000495674.1:n.198-7del
ENST00000643023.1:c.372-7del	ENSP00000495664.1:n.372-7del
ENST00000643584.1:c.372-7del	ENSP00000494987.1:n.372-7del
ENST00000644338.1:c.372-7del	ENSP00000494723.1:n.372-7del
ENST00000646602.1:c.372-7del	ENSP00000495250.1:n.372-7del
ENST00000646804.1:c.198-7del	ENSP00000493977.1:n.198-7del
ENST00000646932.1:c.372-7del MANE Select	ENSP00000494360.1:n.372-7del
ENST00000647361.1:c.*165-7del	ENSP00000494607.1:n.*165-7del
ENST00000378654.8:c.372-7del	ENSP00000367923.3:n.372-7del
ENST00000433022.1:c.90+12470del	ENSP00000415091.1:n.90+12470del
ENST00000434484.5:c.162-7del	ENSP00000392771.1:n.162-7del
ENST00000470760.2:c.372-7del	ENSP00000488974.1:n.372-7del
ENST00000497202.6:c.466-7del	ENSP00000489175.1:n.466-7del
NM_003850.2:c.372-7del	NP_003841.1:n.372-7del
XM_011535292.1:c.135-7del	XP_011533594.1:n.135-7del
XM_011535293.1:c.-31-7del	XP_011533595.1:n.-31-7del
XR_941688.1:n.416-7del
NM_003850.3:c.372-7del MANE Select	NP_003841.1:n.372-7del