Canonical Allele Identifier: CA645594353

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625525_22625526insAG , CM000673.2:g.22625525_22625526insAG GRCh38
NC_000011.9:g.22647071_22647072insAG , CM000673.1:g.22647071_22647072insAG GRCh37
NC_000011.8:g.22603647_22603648insAG NCBI36
NG_007425.1:g.5317_5318insTC , LRG_527:g.5317_5318insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.286_287insTC (FANCF) MANE Select ENSP00000330875.3:p.Arg96LeufsTer?
ENST00000648096.1:n.17_18insAG (GAS2)
ENST00000327470.4:c.286_287insTC (FANCF) ENSP00000330875.3:p.Arg96LeufsTer?
NM_022725.3:c.286_287insTC , LRG_527t1:c.286_287insTC (FANCF) NP_073562.1:p.Arg96LeufsTer?
NM_022725.4:c.286_287insTC (FANCF) MANE Select NP_073562.1:p.Arg96LeufsTer?