Canonical Allele Identifier: CA374109305

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95135411T>A , CM000671.2:g.95135411T>A GRCh38
NC_000009.11:g.97897693T>A , CM000671.1:g.97897693T>A GRCh37
NC_000009.10:g.96937514T>A NCBI36
NG_011707.1:g.187299A>T , LRG_497:g.187299A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.411-11800T>A (AOPEP)
ENST00000696261.1:n.1169A>T (FANCC)
ENST00000289081.8:c.778A>T (FANCC) MANE Select ENSP00000289081.3:p.Lys260Ter
ENST00000375305.6:c.778A>T (FANCC) ENSP00000364454.1:p.Lys260Ter
ENST00000490972.7:c.778A>T (FANCC) ENSP00000479931.1:p.Lys260Ter
ENST00000649334.1:c.923A>T (FANCC) ENSP00000497735.1:n.923A>T
ENST00000649701.1:n.493A>T (FANCC)
ENST00000289081.7:c.778A>T (FANCC) ENSP00000289081.3:p.Lys260Ter
ENST00000375305.5:c.778A>T (FANCC) ENSP00000364454.1:p.Lys260Ter
ENST00000477942.5:n.133A>T (FANCC)
ENST00000490972.6:c.778A>T (FANCC) ENSP00000479931.1:p.Lys260Ter
NM_000136.2:c.778A>T , LRG_497t1:c.778A>T (FANCC) NP_000127.2:p.Lys260Ter
NM_001243743.1:c.778A>T (FANCC) NP_001230672.1:p.Lys260Ter
NM_001243744.1:c.778A>T (FANCC) NP_001230673.1:p.Lys260Ter
XM_005251802.2:c.97A>T (FANCC) XP_005251859.1:p.Lys33Ter
XM_006717001.1:c.613A>T (FANCC) XP_006717064.1:p.Lys205Ter
XM_006717002.2:c.778A>T (FANCC) XP_006717065.1:p.Lys260Ter
XM_006717004.2:c.778A>T (FANCC) XP_006717067.1:p.Lys260Ter
XM_011518365.1:c.778A>T (FANCC) XP_011516667.1:p.Lys260Ter
XM_011518366.1:c.778A>T (FANCC) XP_011516668.1:p.Lys260Ter
XM_011518367.1:c.322A>T (FANCC) XP_011516669.1:p.Lys108Ter
XM_011519121.1:c.2320-11800T>A (AOPEP) XP_011517423.1:n.2320-11800T>A
XM_005251802.3:c.97A>T (FANCC) XP_005251859.1:p.Lys33Ter
XM_006717001.3:c.613A>T (FANCC) XP_006717064.1:p.Lys205Ter
XM_006717002.4:c.778A>T (FANCC) XP_006717065.1:p.Lys260Ter
XM_006717004.4:c.778A>T (FANCC) XP_006717067.1:p.Lys260Ter
XM_011518365.3:c.778A>T (FANCC) XP_011516667.1:p.Lys260Ter
XM_011518366.3:c.778A>T (FANCC) XP_011516668.1:p.Lys260Ter
XM_011518367.2:c.322A>T (FANCC) XP_011516669.1:p.Lys108Ter
XM_011519121.3:c.2320-11800T>A (AOPEP) XP_011517423.1:n.2320-11800T>A
XM_017014452.2:c.322A>T (FANCC) XP_016869941.1:p.Lys108Ter
XM_017014453.1:c.322A>T (FANCC) XP_016869942.1:p.Lys108Ter
XM_017014454.1:c.157A>T (FANCC) XP_016869943.1:p.Lys53Ter
XM_024447451.1:c.778A>T (FANCC) XP_024303219.1:p.Lys260Ter
NM_000136.3:c.778A>T (FANCC) MANE Select NP_000127.2:p.Lys260Ter
NM_001243743.2:c.778A>T (FANCC) NP_001230672.1:p.Lys260Ter
NM_001243744.2:c.778A>T (FANCC) NP_001230673.1:p.Lys260Ter