Canonical Allele Identifier: CA1865483921

Gene: FANCC

Linked Data

• dbSNP Id: rs1825735979

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172248_95172249del , CM000671.2:g.95172248_95172249del	GRCh38
NC_000009.11:g.97934530_97934531del , CM000671.1:g.97934530_97934531del	GRCh37
NC_000009.10:g.96974351_96974352del	NCBI36
NG_011707.1:g.150462_150463del , LRG_497:g.150462_150463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.737-101_737-100del
ENST00000289081.8:c.346-101_346-100del MANE Select	ENSP00000289081.3:n.346-101_346-100del
ENST00000375305.6:c.346-101_346-100del	ENSP00000364454.1:n.346-101_346-100del
ENST00000490972.7:c.346-101_346-100del	ENSP00000479931.1:n.346-101_346-100del
ENST00000636777.1:n.404-101_404-100del
ENST00000647778.1:c.346-101_346-100del	ENSP00000498125.1:n.346-101_346-100del
ENST00000647882.1:c.346-101_346-100del	ENSP00000497025.1:n.346-101_346-100del
ENST00000649334.1:c.491-101_491-100del	ENSP00000497735.1:n.491-101_491-100del
ENST00000649701.1:n.61-101_61-100del
ENST00000289081.7:c.346-101_346-100del	ENSP00000289081.3:n.346-101_346-100del
ENST00000375305.5:c.346-101_346-100del	ENSP00000364454.1:n.346-101_346-100del
ENST00000433829.1:c.346-101_346-100del	ENSP00000406908.1:n.346-101_346-100del
ENST00000474949.1:n.703-101_703-100del
ENST00000490972.6:c.346-101_346-100del	ENSP00000479931.1:n.346-101_346-100del
NM_000136.2:c.346-101_346-100del , LRG_497t1:c.346-101_346-100del	NP_000127.2:n.346-101_346-100del
NM_001243743.1:c.346-101_346-100del	NP_001230672.1:n.346-101_346-100del
NM_001243744.1:c.346-101_346-100del	NP_001230673.1:n.346-101_346-100del
XM_006717001.1:c.346-101_346-100del	XP_006717064.1:n.346-101_346-100del
XM_006717002.2:c.346-101_346-100del	XP_006717065.1:n.346-101_346-100del
XM_006717004.2:c.346-101_346-100del	XP_006717067.1:n.346-101_346-100del
XM_011518365.1:c.346-101_346-100del	XP_011516667.1:n.346-101_346-100del
XM_011518366.1:c.346-101_346-100del	XP_011516668.1:n.346-101_346-100del
XM_011518367.1:c.-111-101_-111-100del	XP_011516669.1:n.-111-101_-111-100del
XM_006717001.3:c.346-101_346-100del	XP_006717064.1:n.346-101_346-100del
XM_006717002.4:c.346-101_346-100del	XP_006717065.1:n.346-101_346-100del
XM_006717004.4:c.346-101_346-100del	XP_006717067.1:n.346-101_346-100del
XM_011518365.3:c.346-101_346-100del	XP_011516667.1:n.346-101_346-100del
XM_011518366.3:c.346-101_346-100del	XP_011516668.1:n.346-101_346-100del
XM_011518367.2:c.-111-101_-111-100del	XP_011516669.1:n.-111-101_-111-100del
XM_017014452.2:c.-111-101_-111-100del	XP_016869941.1:n.-111-101_-111-100del
XM_017014453.1:c.-111-101_-111-100del	XP_016869942.1:n.-111-101_-111-100del
XM_017014454.1:c.-111-101_-111-100del	XP_016869943.1:n.-111-101_-111-100del
XM_024447451.1:c.346-101_346-100del	XP_024303219.1:n.346-101_346-100del
NM_000136.3:c.346-101_346-100del MANE Select	NP_000127.2:n.346-101_346-100del
NM_001243743.2:c.346-101_346-100del	NP_001230672.1:n.346-101_346-100del
NM_001243744.2:c.346-101_346-100del	NP_001230673.1:n.346-101_346-100del