Canonical Allele Identifier: CA2843234982

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95111514del , CM000671.2:g.95111514del GRCh38
NC_000009.11:g.97873796del , CM000671.1:g.97873796del GRCh37
NC_000009.10:g.96913617del NCBI36
NG_011707.1:g.211197del , LRG_497:g.211197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+30734del (AOPEP)
ENST00000696260.1:n.2094del (FANCC)
ENST00000289081.8:c.1279del (FANCC) MANE Select ENSP00000289081.3:p.Ala427ProfsTer20
ENST00000375305.6:c.1279del (FANCC) ENSP00000364454.1:p.Ala427ProfsTer20
ENST00000490972.7:c.1279del (FANCC) ENSP00000479931.1:p.Ala427ProfsTer17
ENST00000649334.1:c.1424del (FANCC) ENSP00000497735.1:n.1424del
ENST00000289081.7:c.1279del (FANCC) ENSP00000289081.3:p.Ala427ProfsTer20
ENST00000375305.5:c.1279del (FANCC) ENSP00000364454.1:p.Ala427ProfsTer20
ENST00000464627.5:n.606del (FANCC)
ENST00000477942.5:n.634del (FANCC)
ENST00000480712.5:n.464del (FANCC)
ENST00000490972.6:c.1279del (FANCC) ENSP00000479931.1:p.Ala427ProfsTer17
NM_000136.2:c.1279del , LRG_497t1:c.1279del (FANCC) NP_000127.2:p.Ala427ProfsTer20
NM_001243743.1:c.1279del (FANCC) NP_001230672.1:p.Ala427ProfsTer20
NM_001243744.1:c.1279del (FANCC) NP_001230673.1:p.Ala427ProfsTer17
XM_005251802.2:c.598del (FANCC) XP_005251859.1:p.Ala200ProfsTer20
XM_006717001.1:c.1114del (FANCC) XP_006717064.1:p.Ala372ProfsTer20
XM_006717002.2:c.1279del (FANCC) XP_006717065.1:p.Ala427ProfsTer25
XM_011518365.1:c.1279del (FANCC) XP_011516667.1:p.Ala427ProfsTer20
XM_011518366.1:c.1279del (FANCC) XP_011516668.1:p.Ala427ProfsTer?
XM_011518367.1:c.823del (FANCC) XP_011516669.1:p.Ala275ProfsTer20
XM_011519121.1:c.2319+30734del (AOPEP) XP_011517423.1:n.2319+30734del
XM_005251802.3:c.598del (FANCC) XP_005251859.1:p.Ala200ProfsTer20
XM_006717001.3:c.1114del (FANCC) XP_006717064.1:p.Ala372ProfsTer20
XM_006717002.4:c.1279del (FANCC) XP_006717065.1:p.Ala427ProfsTer25
XM_011518365.3:c.1279del (FANCC) XP_011516667.1:p.Ala427ProfsTer20
XM_011518366.3:c.1279del (FANCC) XP_011516668.1:p.Ala427ProfsTer?
XM_011518367.2:c.823del (FANCC) XP_011516669.1:p.Ala275ProfsTer20
XM_011519121.3:c.2319+30734del (AOPEP) XP_011517423.1:n.2319+30734del
XM_017014452.2:c.823del (FANCC) XP_016869941.1:p.Ala275ProfsTer20
XM_017014453.1:c.823del (FANCC) XP_016869942.1:p.Ala275ProfsTer20
XM_017014454.1:c.658del (FANCC) XP_016869943.1:p.Ala220ProfsTer20
XM_024447451.1:c.1279del (FANCC) XP_024303219.1:p.Ala427ProfsTer20
NM_000136.3:c.1279del (FANCC) MANE Select NP_000127.2:p.Ala427ProfsTer20
NM_001243743.2:c.1279del (FANCC) NP_001230672.1:p.Ala427ProfsTer20
NM_001243744.2:c.1279del (FANCC) NP_001230673.1:p.Ala427ProfsTer17