Canonical Allele Identifier: CA2622965581

Gene: SUCLA2

Linked Data

• gnomAD v4: 13-47988783-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988783C>G , CM000675.2:g.47988783C>G	GRCh38
NC_000013.10:g.48562918C>G , CM000675.1:g.48562918C>G	GRCh37
NC_000013.9:g.47460919C>G	NCBI36
NG_008241.1:g.17545G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.198-80G>C	ENSP00000495674.1:n.198-80G>C
ENST00000643023.1:c.372-80G>C	ENSP00000495664.1:n.372-80G>C
ENST00000643584.1:c.372-80G>C	ENSP00000494987.1:n.372-80G>C
ENST00000644338.1:c.372-80G>C	ENSP00000494723.1:n.372-80G>C
ENST00000646602.1:c.372-80G>C	ENSP00000495250.1:n.372-80G>C
ENST00000646804.1:c.198-80G>C	ENSP00000493977.1:n.198-80G>C
ENST00000646932.1:c.372-80G>C MANE Select	ENSP00000494360.1:n.372-80G>C
ENST00000647361.1:c.*165-80G>C	ENSP00000494607.1:n.*165-80G>C
ENST00000378654.8:c.372-80G>C	ENSP00000367923.3:n.372-80G>C
ENST00000433022.1:c.90+12397G>C	ENSP00000415091.1:n.90+12397G>C
ENST00000434484.5:c.162-80G>C	ENSP00000392771.1:n.162-80G>C
ENST00000470760.2:c.372-80G>C	ENSP00000488974.1:n.372-80G>C
ENST00000497202.6:c.466-80G>C	ENSP00000489175.1:n.466-80G>C
NM_003850.2:c.372-80G>C	NP_003841.1:n.372-80G>C
XM_011535292.1:c.135-80G>C	XP_011533594.1:n.135-80G>C
XM_011535293.1:c.-31-80G>C	XP_011533595.1:n.-31-80G>C
XR_941688.1:n.416-80G>C
NM_003850.3:c.372-80G>C MANE Select	NP_003841.1:n.372-80G>C