Canonical Allele Identifier: CA9191357
Gene: FDX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10315914C>G , CM000681.2:g.10315914C>G GRCh38
NC_000019.9:g.10426590C>G , CM000681.1:g.10426590C>G GRCh37
NC_000019.8:g.10287590C>G NCBI36
NG_034259.1:g.5102G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706663.1:c.51+32G>C ENSP00000516489.1:n.51+32G>C
ENST00000343376.8:n.100G>C
ENST00000393708.3:c.92G>C MANE Select ENSP00000377311.4:p.Gly31Ala
ENST00000452032.6:c.92G>C ENSP00000408510.2:p.Gly31Ala
ENST00000453681.1:n.97G>C
ENST00000460631.5:n.83G>C
ENST00000486454.1:n.93G>C
ENST00000494368.5:c.-261+56G>C ENSP00000467188.1:n.-261+56G>C
ENST00000586529.1:c.1773+104G>C ENSP00000467814.1:n.1773+104G>C
NM_001031734.3:c.92G>C NP_001026904.2:p.Gly31Ala
NM_001031734.4:c.92G>C NP_001026904.2:p.Gly31Ala
NM_001397406.1:c.83G>C MANE Select NP_001384335.1:p.Gly28Ala