Canonical Allele Identifier: CA2690792294

Gene: FANCC

Linked Data

• gnomAD v4: 9-95172280-CAATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172281_95172284del , CM000671.2:g.95172281_95172284del	GRCh38
NC_000009.11:g.97934563_97934566del , CM000671.1:g.97934563_97934566del	GRCh37
NC_000009.10:g.96974384_96974387del	NCBI36
NG_011707.1:g.150426_150429del , LRG_497:g.150426_150429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.737-137_737-134del
ENST00000289081.8:c.346-137_346-134del MANE Select	ENSP00000289081.3:n.346-137_346-134del
ENST00000375305.6:c.346-137_346-134del	ENSP00000364454.1:n.346-137_346-134del
ENST00000490972.7:c.346-137_346-134del	ENSP00000479931.1:n.346-137_346-134del
ENST00000636777.1:n.404-137_404-134del
ENST00000647778.1:c.346-137_346-134del	ENSP00000498125.1:n.346-137_346-134del
ENST00000647882.1:c.346-137_346-134del	ENSP00000497025.1:n.346-137_346-134del
ENST00000649334.1:c.491-137_491-134del	ENSP00000497735.1:n.491-137_491-134del
ENST00000649701.1:n.61-137_61-134del
ENST00000289081.7:c.346-137_346-134del	ENSP00000289081.3:n.346-137_346-134del
ENST00000375305.5:c.346-137_346-134del	ENSP00000364454.1:n.346-137_346-134del
ENST00000433829.1:c.346-137_346-134del	ENSP00000406908.1:n.346-137_346-134del
ENST00000474949.1:n.703-137_703-134del
ENST00000490972.6:c.346-137_346-134del	ENSP00000479931.1:n.346-137_346-134del
NM_000136.2:c.346-137_346-134del , LRG_497t1:c.346-137_346-134del	NP_000127.2:n.346-137_346-134del
NM_001243743.1:c.346-137_346-134del	NP_001230672.1:n.346-137_346-134del
NM_001243744.1:c.346-137_346-134del	NP_001230673.1:n.346-137_346-134del
XM_006717001.1:c.346-137_346-134del	XP_006717064.1:n.346-137_346-134del
XM_006717002.2:c.346-137_346-134del	XP_006717065.1:n.346-137_346-134del
XM_006717004.2:c.346-137_346-134del	XP_006717067.1:n.346-137_346-134del
XM_011518365.1:c.346-137_346-134del	XP_011516667.1:n.346-137_346-134del
XM_011518366.1:c.346-137_346-134del	XP_011516668.1:n.346-137_346-134del
XM_011518367.1:c.-111-137_-111-134del	XP_011516669.1:n.-111-137_-111-134del
XM_006717001.3:c.346-137_346-134del	XP_006717064.1:n.346-137_346-134del
XM_006717002.4:c.346-137_346-134del	XP_006717065.1:n.346-137_346-134del
XM_006717004.4:c.346-137_346-134del	XP_006717067.1:n.346-137_346-134del
XM_011518365.3:c.346-137_346-134del	XP_011516667.1:n.346-137_346-134del
XM_011518366.3:c.346-137_346-134del	XP_011516668.1:n.346-137_346-134del
XM_011518367.2:c.-111-137_-111-134del	XP_011516669.1:n.-111-137_-111-134del
XM_017014452.2:c.-111-137_-111-134del	XP_016869941.1:n.-111-137_-111-134del
XM_017014453.1:c.-111-137_-111-134del	XP_016869942.1:n.-111-137_-111-134del
XM_017014454.1:c.-111-137_-111-134del	XP_016869943.1:n.-111-137_-111-134del
XM_024447451.1:c.346-137_346-134del	XP_024303219.1:n.346-137_346-134del
NM_000136.3:c.346-137_346-134del MANE Select	NP_000127.2:n.346-137_346-134del
NM_001243743.2:c.346-137_346-134del	NP_001230672.1:n.346-137_346-134del
NM_001243744.2:c.346-137_346-134del	NP_001230673.1:n.346-137_346-134del