Canonical Allele Identifier: CA1999830645
Gene: FDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110460891A= , CM000673.2:g.110460891A= GRCh38
NC_000011.9:g.110331615A= , CM000673.1:g.110331615A= GRCh37
NC_000011.8:g.109836825A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260270.3:c.441-1463A= MANE Select ENSP00000260270.2:n.441-1463A=
ENST00000260270.2:c.441-1463A= ENSP00000260270.2:n.441-1463A=
NM_004109.4:c.441-1463A= NP_004100.1:n.441-1463A=
NM_004109.5:c.441-1463A= MANE Select NP_004100.1:n.441-1463A=
Search 100 bp 5'
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