Canonical Allele Identifier: CA305206386
Gene: FDX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10311209G>C , CM000681.2:g.10311209G>C GRCh38
NC_000019.9:g.10421885G>C , CM000681.1:g.10421885G>C GRCh37
NC_000019.8:g.10282885G>C NCBI36
NG_034259.1:g.9807C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001397406.1:c.308-269C>G MANE Select NP_001384335.1:n.308-269C>G
ENST00000393708.3:c.317-269C>G MANE Select ENSP00000377311.4:n.317-269C>G
NM_001031734.3:c.317-269C>G NP_001026904.2:n.317-269C>G
NM_001031734.4:c.317-269C>G NP_001026904.2:n.317-269C>G
ENST00000343376.8:n.417-269C>G
ENST00000452032.6:c.317-269C>G ENSP00000408510.2:n.317-269C>G
ENST00000453681.1:n.414-269C>G
ENST00000460631.5:n.520-269C>G
ENST00000492239.5:c.-98-269C>G ENSP00000488228.1:n.-98-269C>G
ENST00000493771.2:n.172-269C>G
ENST00000494368.5:c.-98-269C>G ENSP00000467188.1:n.-98-269C>G
ENST00000706663.1:c.52-787C>G ENSP00000516489.1:n.52-787C>G