Canonical Allele Identifier: CA1865515566
Gene: FANCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95249299A= , CM000671.2:g.95249299A= GRCh38
NC_000009.11:g.98011581A= , CM000671.1:g.98011581A= GRCh37
NC_000009.10:g.97051402A= NCBI36
NG_011707.1:g.73411T= , LRG_497:g.73411T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696261.1:n.239T=
ENST00000696262.1:c.-8T= ENSP00000512510.1:n.-8T=
ENST00000696263.1:n.248T=
ENST00000289081.8:c.-8T= MANE Select ENSP00000289081.3:n.-8T=
ENST00000375305.6:c.-8T= ENSP00000364454.1:n.-8T=
ENST00000490972.7:c.-8T= ENSP00000479931.1:n.-8T=
ENST00000636777.1:n.51T=
ENST00000647778.1:c.-8T= ENSP00000498125.1:n.-8T=
ENST00000647882.1:c.-8T= ENSP00000497025.1:n.-8T=
ENST00000648415.1:n.1631T=
ENST00000649519.1:c.-8T= ENSP00000497630.1:n.-8T=
ENST00000649611.1:c.-8T= ENSP00000497986.1:n.-8T=
ENST00000650176.1:n.173T=
ENST00000289081.7:c.-8T= ENSP00000289081.3:n.-8T=
ENST00000375305.5:c.-8T= ENSP00000364454.1:n.-8T=
ENST00000433829.1:c.-8T= ENSP00000406908.1:n.-8T=
ENST00000474949.1:n.255T=
ENST00000490972.6:c.-8T= ENSP00000479931.1:n.-8T=
NM_000136.2:c.-8T= , LRG_497t1:c.-8T= NP_000127.2:n.-8T=
NM_001243743.1:c.-8T= NP_001230672.1:n.-8T=
NM_001243744.1:c.-8T= NP_001230673.1:n.-8T=
XM_006717001.1:c.-8T= XP_006717064.1:n.-8T=
XM_006717002.2:c.-8T= XP_006717065.1:n.-8T=
XM_006717004.2:c.-8T= XP_006717067.1:n.-8T=
XM_011518365.1:c.-8T= XP_011516667.1:n.-8T=
XM_011518366.1:c.-8T= XP_011516668.1:n.-8T=
XM_011518367.1:c.-609T= XP_011516669.1:n.-609T=
XM_006717001.3:c.-8T= XP_006717064.1:n.-8T=
XM_006717002.4:c.-8T= XP_006717065.1:n.-8T=
XM_006717004.4:c.-8T= XP_006717067.1:n.-8T=
XM_011518365.3:c.-8T= XP_011516667.1:n.-8T=
XM_011518366.3:c.-8T= XP_011516668.1:n.-8T=
XM_011518367.2:c.-609T= XP_011516669.1:n.-609T=
XM_017014452.2:c.-609T= XP_016869941.1:n.-609T=
XM_017014453.1:c.-609T= XP_016869942.1:n.-609T=
XM_017014454.1:c.-609T= XP_016869943.1:n.-609T=
XM_024447451.1:c.-8T= XP_024303219.1:n.-8T=
NM_000136.3:c.-8T= MANE Select NP_000127.2:n.-8T=
NM_001243743.2:c.-8T= NP_001230672.1:n.-8T=
NM_001243744.2:c.-8T= NP_001230673.1:n.-8T=