Canonical Allele Identifier: CA2720046304

Gene: FANCC

Linked Data

• dbSNP Id: rs45493695

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171928_95171931dup , CM000671.2:g.95171928_95171931dup	GRCh38
NC_000009.11:g.97934210_97934213dup , CM000671.1:g.97934210_97934213dup	GRCh37
NC_000009.10:g.96974031_96974034dup	NCBI36
NG_011707.1:g.150782_150785dup , LRG_497:g.150782_150785dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.847+109_847+112dup
ENST00000289081.8:c.456+109_456+112dup MANE Select	ENSP00000289081.3:n.456+109_456+112dup
ENST00000375305.6:c.456+109_456+112dup	ENSP00000364454.1:n.456+109_456+112dup
ENST00000490972.7:c.456+109_456+112dup	ENSP00000479931.1:n.456+109_456+112dup
ENST00000636777.1:n.514+109_514+112dup
ENST00000647778.1:c.456+109_456+112dup	ENSP00000498125.1:n.456+109_456+112dup
ENST00000649334.1:c.601+109_601+112dup	ENSP00000497735.1:n.601+109_601+112dup
ENST00000649701.1:n.171+109_171+112dup
ENST00000289081.7:c.456+109_456+112dup	ENSP00000289081.3:n.456+109_456+112dup
ENST00000375305.5:c.456+109_456+112dup	ENSP00000364454.1:n.456+109_456+112dup
ENST00000474949.1:n.813+109_813+112dup
ENST00000490972.6:c.456+109_456+112dup	ENSP00000479931.1:n.456+109_456+112dup
NM_000136.2:c.456+109_456+112dup , LRG_497t1:c.456+109_456+112dup	NP_000127.2:n.456+109_456+112dup
NM_001243743.1:c.456+109_456+112dup	NP_001230672.1:n.456+109_456+112dup
NM_001243744.1:c.456+109_456+112dup	NP_001230673.1:n.456+109_456+112dup
XM_006717001.1:c.456+109_456+112dup	XP_006717064.1:n.456+109_456+112dup
XM_006717002.2:c.456+109_456+112dup	XP_006717065.1:n.456+109_456+112dup
XM_006717004.2:c.456+109_456+112dup	XP_006717067.1:n.456+109_456+112dup
XM_011518365.1:c.456+109_456+112dup	XP_011516667.1:n.456+109_456+112dup
XM_011518366.1:c.456+109_456+112dup	XP_011516668.1:n.456+109_456+112dup
XM_011518367.1:c.-1+109_-1+112dup	XP_011516669.1:n.-1+109_-1+112dup
XM_006717001.3:c.456+109_456+112dup	XP_006717064.1:n.456+109_456+112dup
XM_006717002.4:c.456+109_456+112dup	XP_006717065.1:n.456+109_456+112dup
XM_006717004.4:c.456+109_456+112dup	XP_006717067.1:n.456+109_456+112dup
XM_011518365.3:c.456+109_456+112dup	XP_011516667.1:n.456+109_456+112dup
XM_011518366.3:c.456+109_456+112dup	XP_011516668.1:n.456+109_456+112dup
XM_011518367.2:c.-1+109_-1+112dup	XP_011516669.1:n.-1+109_-1+112dup
XM_017014452.2:c.-1+109_-1+112dup	XP_016869941.1:n.-1+109_-1+112dup
XM_017014453.1:c.-1+109_-1+112dup	XP_016869942.1:n.-1+109_-1+112dup
XM_017014454.1:c.-1+109_-1+112dup	XP_016869943.1:n.-1+109_-1+112dup
XM_024447451.1:c.456+109_456+112dup	XP_024303219.1:n.456+109_456+112dup
NM_000136.3:c.456+109_456+112dup MANE Select	NP_000127.2:n.456+109_456+112dup
NM_001243743.2:c.456+109_456+112dup	NP_001230672.1:n.456+109_456+112dup
NM_001243744.2:c.456+109_456+112dup	NP_001230673.1:n.456+109_456+112dup