Canonical Allele Identifier: CA658821266

Gene: FANCC

Linked Data

• ClinVar Variation Id: 555724
• ClinVar RCV Id: RCV000671594 ; RCV002531291
• dbSNP Id: rs1554858249
• gnomAD v4: 9-95249125-AC-A
• MyVariant Identifiers: chr9:g.95249126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249127del , CM000671.2:g.95249127del	GRCh38
NC_000009.11:g.98011409del , CM000671.1:g.98011409del	GRCh37
NC_000009.10:g.97051230del	NCBI36
NG_011707.1:g.73584del , LRG_497:g.73584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.411+1del
ENST00000696262.1:c.165+1del
ENST00000696263.1:n.421del
ENST00000289081.8:c.165+1del
ENST00000375305.6:c.165+1del
ENST00000490972.7:c.165+1del
ENST00000636777.1:n.223+1del
ENST00000647778.1:c.165+1del
ENST00000647882.1:c.165+1del
ENST00000648415.1:n.1803+1del
ENST00000649334.1:c.165+1del
ENST00000649519.1:c.165+1del
ENST00000649611.1:c.165+1del
ENST00000649872.1:c.165+1del
ENST00000650176.1:n.345+1del
ENST00000289081.7:c.165+1del
ENST00000375305.5:c.165+1del
ENST00000433829.1:c.165+1del
ENST00000474949.1:n.427+1del
ENST00000490972.6:c.165+1del
NM_000136.2:c.165+1del , LRG_497t1:c.165+1del
NM_001243743.1:c.165+1del
NM_001243744.1:c.165+1del
XM_006717001.1:c.165+1del
XM_006717002.2:c.165+1del
XM_006717004.2:c.165+1del
XM_011518365.1:c.165+1del
XM_011518366.1:c.165+1del
XM_011518367.1:c.-437+1del
XM_006717001.3:c.165+1del
XM_006717002.4:c.165+1del
XM_006717004.4:c.165+1del
XM_011518365.3:c.165+1del
XM_011518366.3:c.165+1del
XM_011518367.2:c.-437+1del
XM_017014452.2:c.-437+1del
XM_017014453.1:c.-437+1del
XM_017014454.1:c.-437+1del
XM_024447451.1:c.165+1del
NM_000136.3:c.165+1del
NM_001243743.2:c.165+1del
NM_001243744.2:c.165+1del