Canonical Allele Identifier: CA1865483498

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171966_95171972delinsCCATTTA , CM000671.2:g.95171966_95171972delinsCCATTTA	GRCh38
NC_000009.11:g.97934248_97934254delinsCCATTTA , CM000671.1:g.97934248_97934254delinsCCATTTA	GRCh37
NC_000009.10:g.96974069_96974075delinsCCATTTA	NCBI36
NG_011707.1:g.150738_150744delinsTAAATGG , LRG_497:g.150738_150744delinsTAAATGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696261.1:n.847+65_847+71delinsTAAATGG
ENST00000289081.8:c.456+65_456+71delinsTAAATGG MANE Select	ENSP00000289081.3:n.456+65_456+71delinsTA...
ENST00000375305.6:c.456+65_456+71delinsTAAATGG	ENSP00000364454.1:n.456+65_456+71delinsTA...
ENST00000490972.7:c.456+65_456+71delinsTAAATGG	ENSP00000479931.1:n.456+65_456+71delinsTA...
ENST00000636777.1:n.514+65_514+71delinsTAAATGG
ENST00000647778.1:c.456+65_456+71delinsTAAATGG	ENSP00000498125.1:n.456+65_456+71delinsTA...
ENST00000649334.1:c.601+65_601+71delinsTAAATGG	ENSP00000497735.1:n.601+65_601+71delinsTA...
ENST00000649701.1:n.171+65_171+71delinsTAAATGG
ENST00000289081.7:c.456+65_456+71delinsTAAATGG	ENSP00000289081.3:n.456+65_456+71delinsTA...
ENST00000375305.5:c.456+65_456+71delinsTAAATGG	ENSP00000364454.1:n.456+65_456+71delinsTA...
ENST00000474949.1:n.813+65_813+71delinsTAAATGG
ENST00000490972.6:c.456+65_456+71delinsTAAATGG	ENSP00000479931.1:n.456+65_456+71delinsTA...
NM_000136.2:c.456+65_456+71delinsTAAATGG , LRG_497t1:c.456+65_456+71delinsTAAATGG	NP_000127.2:n.456+65_456+71delinsTAAATGG
NM_001243743.1:c.456+65_456+71delinsTAAATGG	NP_001230672.1:n.456+65_456+71delinsTAAAT...
NM_001243744.1:c.456+65_456+71delinsTAAATGG	NP_001230673.1:n.456+65_456+71delinsTAAAT...
XM_006717001.1:c.456+65_456+71delinsTAAATGG	XP_006717064.1:n.456+65_456+71delinsTAAAT...
XM_006717002.2:c.456+65_456+71delinsTAAATGG	XP_006717065.1:n.456+65_456+71delinsTAAAT...
XM_006717004.2:c.456+65_456+71delinsTAAATGG	XP_006717067.1:n.456+65_456+71delinsTAAAT...
XM_011518365.1:c.456+65_456+71delinsTAAATGG	XP_011516667.1:n.456+65_456+71delinsTAAAT...
XM_011518366.1:c.456+65_456+71delinsTAAATGG	XP_011516668.1:n.456+65_456+71delinsTAAAT...
XM_011518367.1:c.-1+65_-1+71delinsTAAATGG	XP_011516669.1:n.-1+65_-1+71delinsTAAATGG...
XM_006717001.3:c.456+65_456+71delinsTAAATGG	XP_006717064.1:n.456+65_456+71delinsTAAAT...
XM_006717002.4:c.456+65_456+71delinsTAAATGG	XP_006717065.1:n.456+65_456+71delinsTAAAT...
XM_006717004.4:c.456+65_456+71delinsTAAATGG	XP_006717067.1:n.456+65_456+71delinsTAAAT...
XM_011518365.3:c.456+65_456+71delinsTAAATGG	XP_011516667.1:n.456+65_456+71delinsTAAAT...
XM_011518366.3:c.456+65_456+71delinsTAAATGG	XP_011516668.1:n.456+65_456+71delinsTAAAT...
XM_011518367.2:c.-1+65_-1+71delinsTAAATGG	XP_011516669.1:n.-1+65_-1+71delinsTAAATGG...
XM_017014452.2:c.-1+65_-1+71delinsTAAATGG	XP_016869941.1:n.-1+65_-1+71delinsTAAATGG...
XM_017014453.1:c.-1+65_-1+71delinsTAAATGG	XP_016869942.1:n.-1+65_-1+71delinsTAAATGG...
XM_017014454.1:c.-1+65_-1+71delinsTAAATGG	XP_016869943.1:n.-1+65_-1+71delinsTAAATGG...
XM_024447451.1:c.456+65_456+71delinsTAAATGG	XP_024303219.1:n.456+65_456+71delinsTAAAT...
NM_000136.3:c.456+65_456+71delinsTAAATGG MANE Select	NP_000127.2:n.456+65_456+71delinsTAAATGG
NM_001243743.2:c.456+65_456+71delinsTAAATGG	NP_001230672.1:n.456+65_456+71delinsTAAAT...
NM_001243744.2:c.456+65_456+71delinsTAAATGG	NP_001230673.1:n.456+65_456+71delinsTAAAT...