Canonical Allele Identifier: CA2720432694
Gene: FANCC HGNC NCBI

Linked Data

dbSNP Id: rs2135578697

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95171098del , CM000671.2:g.95171098del GRCh38
NC_000009.11:g.97933380del , CM000671.1:g.97933380del GRCh37
NC_000009.10:g.96973201del NCBI36
NG_011707.1:g.151613del , LRG_497:g.151613del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696261.1:n.894del
ENST00000289081.8:c.503del MANE Select ENSP00000289081.3:p.Gly168AspfsTer26
ENST00000375305.6:c.503del ENSP00000364454.1:p.Gly168AspfsTer26
ENST00000490972.7:c.503del ENSP00000479931.1:p.Gly168AspfsTer26
ENST00000636777.1:n.561del
ENST00000649334.1:c.648del ENSP00000497735.1:n.648del
ENST00000649701.1:n.218del
ENST00000289081.7:c.503del ENSP00000289081.3:p.Gly168AspfsTer26
ENST00000375305.5:c.503del ENSP00000364454.1:p.Gly168AspfsTer26
ENST00000490972.6:c.503del ENSP00000479931.1:p.Gly168AspfsTer26
NM_000136.2:c.503del , LRG_497t1:c.503del NP_000127.2:p.Gly168AspfsTer26
NM_001243743.1:c.503del NP_001230672.1:p.Gly168AspfsTer26
NM_001243744.1:c.503del NP_001230673.1:p.Gly168AspfsTer26
XM_006717001.1:c.503del XP_006717064.1:p.Gly168AspfsTer17
XM_006717002.2:c.503del XP_006717065.1:p.Gly168AspfsTer26
XM_006717004.2:c.503del XP_006717067.1:p.Gly168AspfsTer26
XM_011518365.1:c.503del XP_011516667.1:p.Gly168AspfsTer26
XM_011518366.1:c.503del XP_011516668.1:p.Gly168AspfsTer26
XM_011518367.1:c.47del XP_011516669.1:p.Gly16AspfsTer26
XM_006717001.3:c.503del XP_006717064.1:p.Gly168AspfsTer17
XM_006717002.4:c.503del XP_006717065.1:p.Gly168AspfsTer26
XM_006717004.4:c.503del XP_006717067.1:p.Gly168AspfsTer26
XM_011518365.3:c.503del XP_011516667.1:p.Gly168AspfsTer26
XM_011518366.3:c.503del XP_011516668.1:p.Gly168AspfsTer26
XM_011518367.2:c.47del XP_011516669.1:p.Gly16AspfsTer26
XM_017014452.2:c.47del XP_016869941.1:p.Gly16AspfsTer26
XM_017014453.1:c.47del XP_016869942.1:p.Gly16AspfsTer26
XM_017014454.1:c.47del XP_016869943.1:p.Gly16AspfsTer17
XM_024447451.1:c.503del XP_024303219.1:p.Gly168AspfsTer26
NM_000136.3:c.503del MANE Select NP_000127.2:p.Gly168AspfsTer26
NM_001243743.2:c.503del NP_001230672.1:p.Gly168AspfsTer26
NM_001243744.2:c.503del NP_001230673.1:p.Gly168AspfsTer26