Canonical Allele Identifier: CA868770725

Linked Data

dbSNP Id: rs1397326356

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95110965_95110971dup , CM000671.2:g.95110965_95110971dup GRCh38
NC_000009.11:g.97873247_97873253dup , CM000671.1:g.97873247_97873253dup GRCh37
NC_000009.10:g.96913068_96913074dup NCBI36
NG_011707.1:g.211739_211745dup , LRG_497:g.211739_211745dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+30185_410+30191dup (AOPEP)
ENST00000696260.1:n.2144+492_2144+498dup (FANCC)
ENST00000289081.8:c.1329+492_1329+498dup (FANCC) MANE Select ENSP00000289081.3:n.1329+492_1329+498dup
ENST00000375305.6:c.1329+492_1329+498dup (FANCC) ENSP00000364454.1:n.1329+492_1329+498dup
ENST00000490972.7:c.*225_*231dup (FANCC) ENSP00000479931.1:n.*225_*231dup
ENST00000649334.1:c.1474+492_1474+498dup (FANCC) ENSP00000497735.1:n.1474+492_1474+498dup
ENST00000289081.7:c.1329+492_1329+498dup (FANCC) ENSP00000289081.3:n.1329+492_1329+498dup
ENST00000375305.5:c.1329+492_1329+498dup (FANCC) ENSP00000364454.1:n.1329+492_1329+498dup
ENST00000464627.5:n.656+492_656+498dup (FANCC)
ENST00000477942.5:n.684+492_684+498dup (FANCC)
ENST00000480712.5:n.514+492_514+498dup (FANCC)
ENST00000490972.6:c.*225_*231dup (FANCC) ENSP00000479931.1:n.*225_*231dup
NM_000136.2:c.1329+492_1329+498dup , LRG_497t1:c.1329+492_1329+498dup (FANCC) NP_000127.2:n.1329+492_1329+498dup
NM_001243743.1:c.1329+492_1329+498dup (FANCC) NP_001230672.1:n.1329+492_1329+498dup
NM_001243744.1:c.*225_*231dup (FANCC) NP_001230673.1:n.*225_*231dup
XM_005251802.2:c.648+492_648+498dup (FANCC) XP_005251859.1:n.648+492_648+498dup
XM_006717001.1:c.1164+492_1164+498dup (FANCC) XP_006717064.1:n.1164+492_1164+498dup
XM_006717002.2:c.1329+492_1329+498dup (FANCC) XP_006717065.1:n.1329+492_1329+498dup
XM_011518365.1:c.1329+492_1329+498dup (FANCC) XP_011516667.1:n.1329+492_1329+498dup
XM_011518367.1:c.873+492_873+498dup (FANCC) XP_011516669.1:n.873+492_873+498dup
XM_011519121.1:c.2319+30185_2319+30191dup (AOPEP) XP_011517423.1:n.2319+30185_2319+30191dup
XM_005251802.3:c.648+492_648+498dup (FANCC) XP_005251859.1:n.648+492_648+498dup
XM_006717001.3:c.1164+492_1164+498dup (FANCC) XP_006717064.1:n.1164+492_1164+498dup
XM_006717002.4:c.1329+492_1329+498dup (FANCC) XP_006717065.1:n.1329+492_1329+498dup
XM_011518365.3:c.1329+492_1329+498dup (FANCC) XP_011516667.1:n.1329+492_1329+498dup
XM_011518366.3:c.*340_*346dup (FANCC) XP_011516668.1:n.*340_*346dup
XM_011518367.2:c.873+492_873+498dup (FANCC) XP_011516669.1:n.873+492_873+498dup
XM_011519121.3:c.2319+30185_2319+30191dup (AOPEP) XP_011517423.1:n.2319+30185_2319+30191dup
XM_017014452.2:c.873+492_873+498dup (FANCC) XP_016869941.1:n.873+492_873+498dup
XM_017014453.1:c.873+492_873+498dup (FANCC) XP_016869942.1:n.873+492_873+498dup
XM_017014454.1:c.708+492_708+498dup (FANCC) XP_016869943.1:n.708+492_708+498dup
XM_024447451.1:c.1329+492_1329+498dup (FANCC) XP_024303219.1:n.1329+492_1329+498dup
NM_000136.3:c.1329+492_1329+498dup (FANCC) MANE Select NP_000127.2:n.1329+492_1329+498dup
NM_001243743.2:c.1329+492_1329+498dup (FANCC) NP_001230672.1:n.1329+492_1329+498dup
NM_001243744.2:c.*225_*231dup (FANCC) NP_001230673.1:n.*225_*231dup