Canonical Allele Identifier: CA589489202

Gene: FANCC

Linked Data

• ClinVar Variation Id: 526463
• ClinVar RCV Id: RCV000630997 ; RCV001731821
• dbSNP Id: rs1372625836
• gnomAD v2: 9-97933347-AGTTT-A
• gnomAD v3: 9-95171065-AGTTT-A
• gnomAD v4: 9-95171065-AGTTT-A
• MyVariant Identifiers: chr9:g.97933348_97933351del (hg19) ; chr9:g.95171066_95171069del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171066_95171069del , CM000671.2:g.95171066_95171069del	GRCh38
NC_000009.11:g.97933348_97933351del , CM000671.1:g.97933348_97933351del	GRCh37
NC_000009.10:g.96973169_96973172del	NCBI36
NG_011707.1:g.151641_151644del , LRG_497:g.151641_151644del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696261.1:n.912+10_912+13del
ENST00000289081.8:c.521+10_521+13del MANE Select	ENSP00000289081.3:n.521+10_521+13del
ENST00000375305.6:c.521+10_521+13del	ENSP00000364454.1:n.521+10_521+13del
ENST00000490972.7:c.521+10_521+13del	ENSP00000479931.1:n.521+10_521+13del
ENST00000636777.1:n.579+10_579+13del
ENST00000649334.1:c.666+10_666+13del	ENSP00000497735.1:n.666+10_666+13del
ENST00000649701.1:n.236+10_236+13del
ENST00000289081.7:c.521+10_521+13del	ENSP00000289081.3:n.521+10_521+13del
ENST00000375305.5:c.521+10_521+13del	ENSP00000364454.1:n.521+10_521+13del
ENST00000490972.6:c.521+10_521+13del	ENSP00000479931.1:n.521+10_521+13del
NM_000136.2:c.521+10_521+13del , LRG_497t1:c.521+10_521+13del	NP_000127.2:n.521+10_521+13del
NM_001243743.1:c.521+10_521+13del	NP_001230672.1:n.521+10_521+13del
NM_001243744.1:c.521+10_521+13del	NP_001230673.1:n.521+10_521+13del
XM_006717001.1:c.521+10_521+13del	XP_006717064.1:n.521+10_521+13del
XM_006717002.2:c.521+10_521+13del	XP_006717065.1:n.521+10_521+13del
XM_006717004.2:c.521+10_521+13del	XP_006717067.1:n.521+10_521+13del
XM_011518365.1:c.521+10_521+13del	XP_011516667.1:n.521+10_521+13del
XM_011518366.1:c.521+10_521+13del	XP_011516668.1:n.521+10_521+13del
XM_011518367.1:c.65+10_65+13del	XP_011516669.1:n.65+10_65+13del
XM_006717001.3:c.521+10_521+13del	XP_006717064.1:n.521+10_521+13del
XM_006717002.4:c.521+10_521+13del	XP_006717065.1:n.521+10_521+13del
XM_006717004.4:c.521+10_521+13del	XP_006717067.1:n.521+10_521+13del
XM_011518365.3:c.521+10_521+13del	XP_011516667.1:n.521+10_521+13del
XM_011518366.3:c.521+10_521+13del	XP_011516668.1:n.521+10_521+13del
XM_011518367.2:c.65+10_65+13del	XP_011516669.1:n.65+10_65+13del
XM_017014452.2:c.65+10_65+13del	XP_016869941.1:n.65+10_65+13del
XM_017014453.1:c.65+10_65+13del	XP_016869942.1:n.65+10_65+13del
XM_017014454.1:c.65+10_65+13del	XP_016869943.1:n.65+10_65+13del
XM_024447451.1:c.521+10_521+13del	XP_024303219.1:n.521+10_521+13del
NM_000136.3:c.521+10_521+13del MANE Select	NP_000127.2:n.521+10_521+13del
NM_001243743.2:c.521+10_521+13del	NP_001230672.1:n.521+10_521+13del
NM_001243744.2:c.521+10_521+13del	NP_001230673.1:n.521+10_521+13del