Canonical Allele Identifier: CA374338631
Gene: FANCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95171121T>A , CM000671.2:g.95171121T>A GRCh38
NC_000009.11:g.97933403T>A , CM000671.1:g.97933403T>A GRCh37
NC_000009.10:g.96973224T>A NCBI36
NG_011707.1:g.151589A>T , LRG_497:g.151589A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696261.1:n.870A>T
ENST00000289081.8:c.479A>T MANE Select ENSP00000289081.3:p.Glu160Val
ENST00000375305.6:c.479A>T ENSP00000364454.1:p.Glu160Val
ENST00000490972.7:c.479A>T ENSP00000479931.1:p.Glu160Val
ENST00000636777.1:n.537A>T
ENST00000649334.1:c.624A>T ENSP00000497735.1:n.624A>T
ENST00000649701.1:n.194A>T
ENST00000289081.7:c.479A>T ENSP00000289081.3:p.Glu160Val
ENST00000375305.5:c.479A>T ENSP00000364454.1:p.Glu160Val
ENST00000474949.1:n.836A>T
ENST00000490972.6:c.479A>T ENSP00000479931.1:p.Glu160Val
NM_000136.2:c.479A>T , LRG_497t1:c.479A>T NP_000127.2:p.Glu160Val
NM_001243743.1:c.479A>T NP_001230672.1:p.Glu160Val
NM_001243744.1:c.479A>T NP_001230673.1:p.Glu160Val
XM_006717001.1:c.479A>T XP_006717064.1:p.Glu160Val
XM_006717002.2:c.479A>T XP_006717065.1:p.Glu160Val
XM_006717004.2:c.479A>T XP_006717067.1:p.Glu160Val
XM_011518365.1:c.479A>T XP_011516667.1:p.Glu160Val
XM_011518366.1:c.479A>T XP_011516668.1:p.Glu160Val
XM_011518367.1:c.23A>T XP_011516669.1:p.Glu8Val
XM_006717001.3:c.479A>T XP_006717064.1:p.Glu160Val
XM_006717002.4:c.479A>T XP_006717065.1:p.Glu160Val
XM_006717004.4:c.479A>T XP_006717067.1:p.Glu160Val
XM_011518365.3:c.479A>T XP_011516667.1:p.Glu160Val
XM_011518366.3:c.479A>T XP_011516668.1:p.Glu160Val
XM_011518367.2:c.23A>T XP_011516669.1:p.Glu8Val
XM_017014452.2:c.23A>T XP_016869941.1:p.Glu8Val
XM_017014453.1:c.23A>T XP_016869942.1:p.Glu8Val
XM_017014454.1:c.23A>T XP_016869943.1:p.Glu8Val
XM_024447451.1:c.479A>T XP_024303219.1:p.Glu160Val
NM_000136.3:c.479A>T MANE Select NP_000127.2:p.Glu160Val
NM_001243743.2:c.479A>T NP_001230672.1:p.Glu160Val
NM_001243744.2:c.479A>T NP_001230673.1:p.Glu160Val