Canonical Allele Identifier: CA1139660974
Gene: FANCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35078670dup , CM000671.2:g.35078670dup GRCh38
NC_000009.11:g.35078667dup , CM000671.1:g.35078667dup GRCh37
NC_000009.10:g.35068667dup NCBI36
NG_007312.1:g.6349dup , LRG_499:g.6349dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000448890.2:c.244dup ENSP00000409607.2:p.Ala82GlyfsTer?
ENST00000461149.2:n.720dup
ENST00000696700.1:n.494dup
ENST00000696701.1:n.459dup
ENST00000696702.1:c.244dup ENSP00000512821.1:p.Ala82GlyfsTer?
ENST00000696703.1:c.244dup ENSP00000512822.1:p.Ala82GlyfsTer?
ENST00000696706.1:n.307dup
ENST00000696707.1:n.200dup
ENST00000696708.1:c.244dup ENSP00000512825.1:p.Ala82GlyfsTer?
ENST00000696709.1:n.646dup
ENST00000696710.1:c.244dup ENSP00000512826.1:p.Ala82GlyfsTer?
ENST00000696711.1:n.591dup
ENST00000696713.1:c.244dup ENSP00000512827.1:p.Ala82GlyfsTer?
ENST00000696714.1:n.923dup
ENST00000696715.1:c.244dup ENSP00000512828.1:p.Ala82GlyfsTer?
ENST00000378643.8:c.244dup MANE Select ENSP00000367910.4:p.Ala82GlyfsTer?
ENST00000378643.7:c.244dup ENSP00000367910.3:p.Ala82GlyfsTer?
ENST00000425676.5:c.244dup ENSP00000412793.1:p.Ala82GlyfsTer?
ENST00000448890.1:c.244dup ENSP00000409607.1:p.Ala82GlyfsTer?
ENST00000462124.1:n.588dup
NM_004629.1:c.244dup , LRG_499t1:c.244dup NP_004620.1:p.Ala82GlyfsTer?
NM_004629.2:c.244dup MANE Select NP_004620.1:p.Ala82GlyfsTer?