Canonical Allele Identifier: CA1139660973
Gene: FANCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35078666del , CM000671.2:g.35078666del GRCh38
NC_000009.11:g.35078663del , CM000671.1:g.35078663del GRCh37
NC_000009.10:g.35068663del NCBI36
NG_007312.1:g.6352del , LRG_499:g.6352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000448890.2:c.247del ENSP00000409607.2:p.Ser83AlafsTer18
ENST00000461149.2:n.723del
ENST00000696700.1:n.497del
ENST00000696701.1:n.462del
ENST00000696702.1:c.247del ENSP00000512821.1:p.Ser83AlafsTer18
ENST00000696703.1:c.247del ENSP00000512822.1:p.Ser83AlafsTer18
ENST00000696706.1:n.310del
ENST00000696707.1:n.203del
ENST00000696708.1:c.247del ENSP00000512825.1:p.Ser83AlafsTer18
ENST00000696709.1:n.649del
ENST00000696710.1:c.247del ENSP00000512826.1:p.Ser83AlafsTer18
ENST00000696711.1:n.594del
ENST00000696713.1:c.247del ENSP00000512827.1:p.Ser83AlafsTer18
ENST00000696714.1:n.926del
ENST00000696715.1:c.247del ENSP00000512828.1:p.Ser83AlafsTer18
ENST00000378643.8:c.247del MANE Select ENSP00000367910.4:p.Ser83AlafsTer18
ENST00000378643.7:c.247del ENSP00000367910.3:p.Ser83AlafsTer18
ENST00000425676.5:c.247del ENSP00000412793.1:p.Ser83AlafsTer18
ENST00000448890.1:c.247del ENSP00000409607.1:p.Ser83AlafsTer18
ENST00000462124.1:n.591del
NM_004629.1:c.247del , LRG_499t1:c.247del NP_004620.1:p.Ser83AlafsTer18
NM_004629.2:c.247del MANE Select NP_004620.1:p.Ser83AlafsTer18