Canonical Allele Identifier: CA1139661051

Linked Data

ClinVar Variation Id: 929818
ClinVar RCV Id: RCV001195059
dbSNP Id: rs2071089000

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95101834dup , CM000671.2:g.95101834dup GRCh38
NC_000009.11:g.97864116dup , CM000671.1:g.97864116dup GRCh37
NC_000009.10:g.96903937dup NCBI36
NG_011707.1:g.220876dup , LRG_497:g.220876dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+21054dup (AOPEP)
ENST00000696260.1:n.2365dup (FANCC)
ENST00000289081.8:c.1550dup (FANCC) MANE Select ENSP00000289081.3:p.Ile518AspfsTer10
ENST00000375305.6:c.1550dup (FANCC) ENSP00000364454.1:p.Ile518AspfsTer10
ENST00000649334.1:c.1695dup (FANCC) ENSP00000497735.1:n.1695dup
ENST00000289081.7:c.1550dup (FANCC) ENSP00000289081.3:p.Ile518AspfsTer10
ENST00000375305.5:c.1550dup (FANCC) ENSP00000364454.1:p.Ile518AspfsTer10
NM_000136.2:c.1550dup , LRG_497t1:c.1550dup (FANCC) NP_000127.2:p.Ile518AspfsTer10
NM_001243743.1:c.1550dup (FANCC) NP_001230672.1:p.Ile518AspfsTer10
XM_005251802.2:c.869dup (FANCC) XP_005251859.1:p.Ile291AspfsTer10
XM_006717001.1:c.1385dup (FANCC) XP_006717064.1:p.Ile463AspfsTer10
XM_011518365.1:c.1550dup (FANCC) XP_011516667.1:p.Ile518AspfsTer10
XM_011518367.1:c.1094dup (FANCC) XP_011516669.1:p.Ile366AspfsTer10
XM_011519121.1:c.2319+21054dup (AOPEP) XP_011517423.1:n.2319+21054dup
XM_005251802.3:c.869dup (FANCC) XP_005251859.1:p.Ile291AspfsTer10
XM_006717001.3:c.1385dup (FANCC) XP_006717064.1:p.Ile463AspfsTer10
XM_011518365.3:c.1550dup (FANCC) XP_011516667.1:p.Ile518AspfsTer10
XM_011518367.2:c.1094dup (FANCC) XP_011516669.1:p.Ile366AspfsTer10
XM_011519121.3:c.2319+21054dup (AOPEP) XP_011517423.1:n.2319+21054dup
XM_017014452.2:c.1094dup (FANCC) XP_016869941.1:p.Ile366AspfsTer10
XM_017014453.1:c.1094dup (FANCC) XP_016869942.1:p.Ile366AspfsTer10
XM_017014454.1:c.929dup (FANCC) XP_016869943.1:p.Ile311AspfsTer10
XM_024447451.1:c.1550dup (FANCC) XP_024303219.1:p.Ile518AspfsTer10
NM_000136.3:c.1550dup (FANCC) MANE Select NP_000127.2:p.Ile518AspfsTer10
NM_001243743.2:c.1550dup (FANCC) NP_001230672.1:p.Ile518AspfsTer10