Canonical Allele Identifier: CA1865429421

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95125092G= , CM000671.2:g.95125092G= GRCh38
NC_000009.11:g.97887374G= , CM000671.1:g.97887374G= GRCh37
NC_000009.10:g.96927195G= NCBI36
NG_011707.1:g.197618C= , LRG_497:g.197618C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.411-22119G= (AOPEP)
ENST00000289081.8:c.990C= (FANCC) MANE Select ENSP00000289081.3:p.Ser330=
ENST00000375305.6:c.990C= (FANCC) ENSP00000364454.1:p.Ser330=
ENST00000490972.7:c.990C= (FANCC) ENSP00000479931.1:p.Ser330=
ENST00000649334.1:c.1135C= (FANCC) ENSP00000497735.1:n.1135C=
ENST00000289081.7:c.990C= (FANCC) ENSP00000289081.3:p.Ser330=
ENST00000375305.5:c.990C= (FANCC) ENSP00000364454.1:p.Ser330=
ENST00000464627.5:n.317C= (FANCC)
ENST00000464653.1:n.986C= (FANCC)
ENST00000477942.5:n.345C= (FANCC)
ENST00000480712.5:n.175C= (FANCC)
ENST00000490972.6:c.990C= (FANCC) ENSP00000479931.1:p.Ser330=
NM_000136.2:c.990C= , LRG_497t1:c.990C= (FANCC) NP_000127.2:p.Ser330=
NM_001243743.1:c.990C= (FANCC) NP_001230672.1:p.Ser330=
NM_001243744.1:c.990C= (FANCC) NP_001230673.1:p.Ser330=
XM_005251802.2:c.309C= (FANCC) XP_005251859.1:p.Ser103=
XM_006717001.1:c.825C= (FANCC) XP_006717064.1:p.Ser275=
XM_006717002.2:c.990C= (FANCC) XP_006717065.1:p.Ser330=
XM_006717004.2:c.990C= (FANCC) XP_006717067.1:p.Ser330=
XM_011518365.1:c.990C= (FANCC) XP_011516667.1:p.Ser330=
XM_011518366.1:c.990C= (FANCC) XP_011516668.1:p.Ser330=
XM_011518367.1:c.534C= (FANCC) XP_011516669.1:p.Ser178=
XM_011519121.1:c.2320-22119G= (AOPEP) XP_011517423.1:n.2320-22119G=
XM_005251802.3:c.309C= (FANCC) XP_005251859.1:p.Ser103=
XM_006717001.3:c.825C= (FANCC) XP_006717064.1:p.Ser275=
XM_006717002.4:c.990C= (FANCC) XP_006717065.1:p.Ser330=
XM_006717004.4:c.990C= (FANCC) XP_006717067.1:p.Ser330=
XM_011518365.3:c.990C= (FANCC) XP_011516667.1:p.Ser330=
XM_011518366.3:c.990C= (FANCC) XP_011516668.1:p.Ser330=
XM_011518367.2:c.534C= (FANCC) XP_011516669.1:p.Ser178=
XM_011519121.3:c.2320-22119G= (AOPEP) XP_011517423.1:n.2320-22119G=
XM_017014452.2:c.534C= (FANCC) XP_016869941.1:p.Ser178=
XM_017014453.1:c.534C= (FANCC) XP_016869942.1:p.Ser178=
XM_017014454.1:c.369C= (FANCC) XP_016869943.1:p.Ser123=
XM_024447451.1:c.990C= (FANCC) XP_024303219.1:p.Ser330=
NM_000136.3:c.990C= (FANCC) MANE Select NP_000127.2:p.Ser330=
NM_001243743.2:c.990C= (FANCC) NP_001230672.1:p.Ser330=
NM_001243744.2:c.990C= (FANCC) NP_001230673.1:p.Ser330=