Canonical Allele Identifier: CA1865483222

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171371_95171375delinsTAGAC , CM000671.2:g.95171371_95171375delinsTAGAC	GRCh38
NC_000009.11:g.97933653_97933657delinsTAGAC , CM000671.1:g.97933653_97933657delinsTAGAC	GRCh37
NC_000009.10:g.96973474_96973478delinsTAGAC	NCBI36
NG_011707.1:g.151335_151339delinsGTCTA , LRG_497:g.151335_151339delinsGTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.848-232_848-228delinsGTCTA
ENST00000289081.8:c.457-232_457-228delinsGTCTA MANE Select	ENSP00000289081.3:n.457-232_457-228delinsGTCTA
ENST00000375305.6:c.457-232_457-228delinsGTCTA	ENSP00000364454.1:n.457-232_457-228delinsGTCTA
ENST00000490972.7:c.457-232_457-228delinsGTCTA	ENSP00000479931.1:n.457-232_457-228delinsGTCTA
ENST00000636777.1:n.515-232_515-228delinsGTCTA
ENST00000647778.1:c.457-232_457-228delinsGTCTA	ENSP00000498125.1:n.457-232_457-228delinsGTCTA
ENST00000649334.1:c.602-232_602-228delinsGTCTA	ENSP00000497735.1:n.602-232_602-228delinsGTCTA
ENST00000649701.1:n.172-232_172-228delinsGTCTA
ENST00000289081.7:c.457-232_457-228delinsGTCTA	ENSP00000289081.3:n.457-232_457-228delinsGTCTA
ENST00000375305.5:c.457-232_457-228delinsGTCTA	ENSP00000364454.1:n.457-232_457-228delinsGTCTA
ENST00000474949.1:n.814-232_814-228delinsGTCTA
ENST00000490972.6:c.457-232_457-228delinsGTCTA	ENSP00000479931.1:n.457-232_457-228delinsGTCTA
NM_000136.2:c.457-232_457-228delinsGTCTA , LRG_497t1:c.457-232_457-228delinsGTCTA	NP_000127.2:n.457-232_457-228delinsGTCTA
NM_001243743.1:c.457-232_457-228delinsGTCTA	NP_001230672.1:n.457-232_457-228delinsGTCTA
NM_001243744.1:c.457-232_457-228delinsGTCTA	NP_001230673.1:n.457-232_457-228delinsGTCTA
XM_006717001.1:c.457-232_457-228delinsGTCTA	XP_006717064.1:n.457-232_457-228delinsGTCTA
XM_006717002.2:c.457-232_457-228delinsGTCTA	XP_006717065.1:n.457-232_457-228delinsGTCTA
XM_006717004.2:c.457-232_457-228delinsGTCTA	XP_006717067.1:n.457-232_457-228delinsGTCTA
XM_011518365.1:c.457-232_457-228delinsGTCTA	XP_011516667.1:n.457-232_457-228delinsGTCTA
XM_011518366.1:c.457-232_457-228delinsGTCTA	XP_011516668.1:n.457-232_457-228delinsGTCTA
XM_011518367.1:c.1-232_1-228delinsGTCTA	XP_011516669.1:n.1-232_1-228delinsGTCTA
XM_006717001.3:c.457-232_457-228delinsGTCTA	XP_006717064.1:n.457-232_457-228delinsGTCTA
XM_006717002.4:c.457-232_457-228delinsGTCTA	XP_006717065.1:n.457-232_457-228delinsGTCTA
XM_006717004.4:c.457-232_457-228delinsGTCTA	XP_006717067.1:n.457-232_457-228delinsGTCTA
XM_011518365.3:c.457-232_457-228delinsGTCTA	XP_011516667.1:n.457-232_457-228delinsGTCTA
XM_011518366.3:c.457-232_457-228delinsGTCTA	XP_011516668.1:n.457-232_457-228delinsGTCTA
XM_011518367.2:c.1-232_1-228delinsGTCTA	XP_011516669.1:n.1-232_1-228delinsGTCTA
XM_017014452.2:c.1-232_1-228delinsGTCTA	XP_016869941.1:n.1-232_1-228delinsGTCTA
XM_017014453.1:c.1-232_1-228delinsGTCTA	XP_016869942.1:n.1-232_1-228delinsGTCTA
XM_017014454.1:c.1-232_1-228delinsGTCTA	XP_016869943.1:n.1-232_1-228delinsGTCTA
XM_024447451.1:c.457-232_457-228delinsGTCTA	XP_024303219.1:n.457-232_457-228delinsGTCTA
NM_000136.3:c.457-232_457-228delinsGTCTA MANE Select	NP_000127.2:n.457-232_457-228delinsGTCTA
NM_001243743.2:c.457-232_457-228delinsGTCTA	NP_001230672.1:n.457-232_457-228delinsGTCTA
NM_001243744.2:c.457-232_457-228delinsGTCTA	NP_001230673.1:n.457-232_457-228delinsGTCTA