Canonical Allele Identifier: CA2720433396
Gene: FANCC HGNC NCBI

Linked Data

dbSNP Id: rs2135579748

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95171141_95171152del , CM000671.2:g.95171141_95171152del GRCh38
NC_000009.11:g.97933423_97933434del , CM000671.1:g.97933423_97933434del GRCh37
NC_000009.10:g.96973244_96973255del NCBI36
NG_011707.1:g.151564_151575del , LRG_497:g.151564_151575del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696261.1:n.848-3_856del
ENST00000289081.8:c.457-3_465del
ENST00000375305.6:c.457-3_465del
ENST00000490972.7:c.457-3_465del
ENST00000636777.1:n.515-3_523del
ENST00000649334.1:c.602-3_610del
ENST00000649701.1:n.172-3_180del
ENST00000289081.7:c.457-3_465del
ENST00000375305.5:c.457-3_465del
ENST00000474949.1:n.814-3_822del
ENST00000490972.6:c.457-3_465del
NM_000136.2:c.457-3_465del , LRG_497t1:c.457-3_465del
NM_001243743.1:c.457-3_465del
NM_001243744.1:c.457-3_465del
XM_006717001.1:c.457-3_465del
XM_006717002.2:c.457-3_465del
XM_006717004.2:c.457-3_465del
XM_011518365.1:c.457-3_465del
XM_011518366.1:c.457-3_465del
XM_011518367.1:c.1-3_9del
XM_006717001.3:c.457-3_465del
XM_006717002.4:c.457-3_465del
XM_006717004.4:c.457-3_465del
XM_011518365.3:c.457-3_465del
XM_011518366.3:c.457-3_465del
XM_011518367.2:c.1-3_9del
XM_017014452.2:c.1-3_9del
XM_017014453.1:c.1-3_9del
XM_017014454.1:c.1-3_9del
XM_024447451.1:c.457-3_465del
NM_000136.3:c.457-3_465del
NM_001243743.2:c.457-3_465del
NM_001243744.2:c.457-3_465del