Canonical Allele Identifier: CA2785167584

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95111499dup , CM000671.2:g.95111499dup GRCh38
NC_000009.11:g.97873781dup , CM000671.1:g.97873781dup GRCh37
NC_000009.10:g.96913602dup NCBI36
NG_011707.1:g.211215dup , LRG_497:g.211215dup

Transcript Alleles

HGVS Amino-acid change
ENST00000710812.1:n.410+30719dup (AOPEP)
ENST00000696260.1:n.2112dup (FANCC)
ENST00000289081.8:c.1297dup (FANCC) MANE Select ENSP00000289081.3:p.Arg433ProfsTer2
ENST00000375305.6:c.1297dup (FANCC) ENSP00000364454.1:p.Arg433ProfsTer2
ENST00000490972.7:c.1297dup (FANCC) ENSP00000479931.1:p.Arg433ProfsTer2
ENST00000649334.1:c.1442dup (FANCC) ENSP00000497735.1:n.1442dup
ENST00000289081.7:c.1297dup (FANCC) ENSP00000289081.3:p.Arg433ProfsTer2
ENST00000375305.5:c.1297dup (FANCC) ENSP00000364454.1:p.Arg433ProfsTer2
ENST00000464627.5:n.624dup (FANCC)
ENST00000477942.5:n.652dup (FANCC)
ENST00000480712.5:n.482dup (FANCC)
ENST00000490972.6:c.1297dup (FANCC) ENSP00000479931.1:p.Arg433ProfsTer2
NM_000136.2:c.1297dup , LRG_497t1:c.1297dup (FANCC) NP_000127.2:p.Arg433ProfsTer2
NM_001243743.1:c.1297dup (FANCC) NP_001230672.1:p.Arg433ProfsTer2
NM_001243744.1:c.1297dup (FANCC) NP_001230673.1:p.Arg433ProfsTer2
XM_005251802.2:c.616dup (FANCC) XP_005251859.1:p.Arg206ProfsTer2
XM_006717001.1:c.1132dup (FANCC) XP_006717064.1:p.Arg378ProfsTer2
XM_006717002.2:c.1297dup (FANCC) XP_006717065.1:p.Arg433ProfsTer2
XM_011518365.1:c.1297dup (FANCC) XP_011516667.1:p.Arg433ProfsTer2
XM_011518366.1:c.1297dup (FANCC) XP_011516668.1:p.Arg433ProfsTer2
XM_011518367.1:c.841dup (FANCC) XP_011516669.1:p.Arg281ProfsTer2
XM_011519121.1:c.2319+30719dup (AOPEP) XP_011517423.1:n.2319+30719dup
XM_005251802.3:c.616dup (FANCC) XP_005251859.1:p.Arg206ProfsTer2
XM_006717001.3:c.1132dup (FANCC) XP_006717064.1:p.Arg378ProfsTer2
XM_006717002.4:c.1297dup (FANCC) XP_006717065.1:p.Arg433ProfsTer2
XM_011518365.3:c.1297dup (FANCC) XP_011516667.1:p.Arg433ProfsTer2
XM_011518366.3:c.1297dup (FANCC) XP_011516668.1:p.Arg433ProfsTer2
XM_011518367.2:c.841dup (FANCC) XP_011516669.1:p.Arg281ProfsTer2
XM_011519121.3:c.2319+30719dup (AOPEP) XP_011517423.1:n.2319+30719dup
XM_017014452.2:c.841dup (FANCC) XP_016869941.1:p.Arg281ProfsTer2
XM_017014453.1:c.841dup (FANCC) XP_016869942.1:p.Arg281ProfsTer2
XM_017014454.1:c.676dup (FANCC) XP_016869943.1:p.Arg226ProfsTer2
XM_024447451.1:c.1297dup (FANCC) XP_024303219.1:p.Arg433ProfsTer2
NM_000136.3:c.1297dup (FANCC) MANE Select NP_000127.2:p.Arg433ProfsTer2
NM_001243743.2:c.1297dup (FANCC) NP_001230672.1:p.Arg433ProfsTer2
NM_001243744.2:c.1297dup (FANCC) NP_001230673.1:p.Arg433ProfsTer2