Canonical Allele Identifier: CA427119087
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84658725C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84431601C>T , CM000664.2:g.84431601C>T GRCh38
NC_000002.11:g.84658725C>T , CM000664.1:g.84658725C>T GRCh37
NC_000002.10:g.84512236C>T NCBI36
NG_016755.1:g.32862G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.732G>A MANE Select ENSP00000377446.2:p.Leu244=
ENST00000651342.1:c.*172G>A ENSP00000498471.1:n.*172G>A
ENST00000393868.6:c.732G>A ENSP00000377446.2:p.Leu244=
ENST00000487809.1:n.479G>A
ENST00000491123.5:n.578G>A
NM_003849.3:c.732G>A NP_003840.2:p.Leu244=
NM_003849.4:c.732G>A MANE Select NP_003840.2:p.Leu244=