Canonical Allele Identifier: CA374338568
Gene: FANCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95171093A>C , CM000671.2:g.95171093A>C GRCh38
NC_000009.11:g.97933375A>C , CM000671.1:g.97933375A>C GRCh37
NC_000009.10:g.96973196A>C NCBI36
NG_011707.1:g.151617T>G , LRG_497:g.151617T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696261.1:n.898T>G
ENST00000289081.8:c.507T>G MANE Select ENSP00000289081.3:p.Phe169Leu
ENST00000375305.6:c.507T>G ENSP00000364454.1:p.Phe169Leu
ENST00000490972.7:c.507T>G ENSP00000479931.1:p.Phe169Leu
ENST00000636777.1:n.565T>G
ENST00000649334.1:c.652T>G ENSP00000497735.1:n.652T>G
ENST00000649701.1:n.222T>G
ENST00000289081.7:c.507T>G ENSP00000289081.3:p.Phe169Leu
ENST00000375305.5:c.507T>G ENSP00000364454.1:p.Phe169Leu
ENST00000490972.6:c.507T>G ENSP00000479931.1:p.Phe169Leu
NM_000136.2:c.507T>G , LRG_497t1:c.507T>G NP_000127.2:p.Phe169Leu
NM_001243743.1:c.507T>G NP_001230672.1:p.Phe169Leu
NM_001243744.1:c.507T>G NP_001230673.1:p.Phe169Leu
XM_006717001.1:c.507T>G XP_006717064.1:p.Phe169Leu
XM_006717002.2:c.507T>G XP_006717065.1:p.Phe169Leu
XM_006717004.2:c.507T>G XP_006717067.1:p.Phe169Leu
XM_011518365.1:c.507T>G XP_011516667.1:p.Phe169Leu
XM_011518366.1:c.507T>G XP_011516668.1:p.Phe169Leu
XM_011518367.1:c.51T>G XP_011516669.1:p.Phe17Leu
XM_006717001.3:c.507T>G XP_006717064.1:p.Phe169Leu
XM_006717002.4:c.507T>G XP_006717065.1:p.Phe169Leu
XM_006717004.4:c.507T>G XP_006717067.1:p.Phe169Leu
XM_011518365.3:c.507T>G XP_011516667.1:p.Phe169Leu
XM_011518366.3:c.507T>G XP_011516668.1:p.Phe169Leu
XM_011518367.2:c.51T>G XP_011516669.1:p.Phe17Leu
XM_017014452.2:c.51T>G XP_016869941.1:p.Phe17Leu
XM_017014453.1:c.51T>G XP_016869942.1:p.Phe17Leu
XM_017014454.1:c.51T>G XP_016869943.1:p.Phe17Leu
XM_024447451.1:c.507T>G XP_024303219.1:p.Phe169Leu
NM_000136.3:c.507T>G MANE Select NP_000127.2:p.Phe169Leu
NM_001243743.2:c.507T>G NP_001230672.1:p.Phe169Leu
NM_001243744.2:c.507T>G NP_001230673.1:p.Phe169Leu