Canonical Allele Identifier: CA658657877

Gene: FANCC

Linked Data

• ClinVar Variation Id: 456162
• ClinVar RCV Id: RCV000557382
• dbSNP Id: rs1554858333
• MyVariant Identifiers: chr9:g.98011538_98011540del (hg19) ; chr9:g.95249256_95249258del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249258_95249260del , CM000671.2:g.95249258_95249260del	GRCh38
NC_000009.11:g.98011540_98011542del , CM000671.1:g.98011540_98011542del	GRCh37
NC_000009.10:g.97051361_97051363del	NCBI36
NG_011707.1:g.73452_73454del , LRG_497:g.73452_73454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.280_282del
ENST00000696262.1:c.34_36del	ENSP00000512510.1:p.Tyr12del
ENST00000696263.1:n.289_291del
ENST00000289081.8:c.34_36del MANE Select	ENSP00000289081.3:p.Tyr12del
ENST00000375305.6:c.34_36del	ENSP00000364454.1:p.Tyr12del
ENST00000490972.7:c.34_36del	ENSP00000479931.1:p.Tyr12del
ENST00000636777.1:n.92_94del
ENST00000647778.1:c.34_36del	ENSP00000498125.1:p.Tyr12del
ENST00000647882.1:c.34_36del	ENSP00000497025.1:p.Tyr12del
ENST00000648415.1:n.1672_1674del
ENST00000649334.1:c.34_36del	ENSP00000497735.1:p.Tyr12del
ENST00000649519.1:c.34_36del	ENSP00000497630.1:p.Tyr12del
ENST00000649611.1:c.34_36del	ENSP00000497986.1:p.Tyr12del
ENST00000649872.1:c.34_36del	ENSP00000497195.1:p.Tyr12del
ENST00000650176.1:n.214_216del
ENST00000289081.7:c.34_36del	ENSP00000289081.3:p.Tyr12del
ENST00000375305.5:c.34_36del	ENSP00000364454.1:p.Tyr12del
ENST00000433829.1:c.34_36del	ENSP00000406908.1:p.Tyr12del
ENST00000474949.1:n.296_298del
ENST00000490972.6:c.34_36del	ENSP00000479931.1:p.Tyr12del
NM_000136.2:c.34_36del , LRG_497t1:c.34_36del	NP_000127.2:p.Tyr12del
NM_001243743.1:c.34_36del	NP_001230672.1:p.Tyr12del
NM_001243744.1:c.34_36del	NP_001230673.1:p.Tyr12del
XM_006717001.1:c.34_36del	XP_006717064.1:p.Tyr12del
XM_006717002.2:c.34_36del	XP_006717065.1:p.Tyr12del
XM_006717004.2:c.34_36del	XP_006717067.1:p.Tyr12del
XM_011518365.1:c.34_36del	XP_011516667.1:p.Tyr12del
XM_011518366.1:c.34_36del	XP_011516668.1:p.Tyr12del
XM_011518367.1:c.-568_-566del	XP_011516669.1:n.-568_-566del
XM_006717001.3:c.34_36del	XP_006717064.1:p.Tyr12del
XM_006717002.4:c.34_36del	XP_006717065.1:p.Tyr12del
XM_006717004.4:c.34_36del	XP_006717067.1:p.Tyr12del
XM_011518365.3:c.34_36del	XP_011516667.1:p.Tyr12del
XM_011518366.3:c.34_36del	XP_011516668.1:p.Tyr12del
XM_011518367.2:c.-568_-566del	XP_011516669.1:n.-568_-566del
XM_017014452.2:c.-568_-566del	XP_016869941.1:n.-568_-566del
XM_017014453.1:c.-568_-566del	XP_016869942.1:n.-568_-566del
XM_017014454.1:c.-568_-566del	XP_016869943.1:n.-568_-566del
XM_024447451.1:c.34_36del	XP_024303219.1:p.Tyr12del
NM_000136.3:c.34_36del MANE Select	NP_000127.2:p.Tyr12del
NM_001243743.2:c.34_36del	NP_001230672.1:p.Tyr12del
NM_001243744.2:c.34_36del	NP_001230673.1:p.Tyr12del