Canonical Allele Identifier: CA2544794948

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171424_95171425insAGAACTGATG , CM000671.2:g.95171424_95171425insAGAACTGATG	GRCh38
NC_000009.11:g.97933706_97933707insAGAACTGATG , CM000671.1:g.97933706_97933707insAGAACTGATG	GRCh37
NC_000009.10:g.96973527_96973528insAGAACTGATG	NCBI36
NG_011707.1:g.151285_151286insCATCAGTTCT , LRG_497:g.151285_151286insCATCAGTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.848-282_848-281insCATCAGTTCT
ENST00000289081.8:c.457-282_457-281insCATCAGTTCT MANE Select	ENSP00000289081.3:n.457-282_457-281insCATCAGTTCT
ENST00000375305.6:c.457-282_457-281insCATCAGTTCT	ENSP00000364454.1:n.457-282_457-281insCATCAGTTCT
ENST00000490972.7:c.457-282_457-281insCATCAGTTCT	ENSP00000479931.1:n.457-282_457-281insCATCAGTTCT
ENST00000636777.1:n.515-282_515-281insCATCAGTTCT
ENST00000647778.1:c.457-282_457-281insCATCAGTTCT	ENSP00000498125.1:n.457-282_457-281insCATCAGTTCT
ENST00000649334.1:c.602-282_602-281insCATCAGTTCT	ENSP00000497735.1:n.602-282_602-281insCATCAGTTCT
ENST00000649701.1:n.172-282_172-281insCATCAGTTCT
ENST00000289081.7:c.457-282_457-281insCATCAGTTCT	ENSP00000289081.3:n.457-282_457-281insCATCAGTTCT
ENST00000375305.5:c.457-282_457-281insCATCAGTTCT	ENSP00000364454.1:n.457-282_457-281insCATCAGTTCT
ENST00000474949.1:n.814-282_814-281insCATCAGTTCT
ENST00000490972.6:c.457-282_457-281insCATCAGTTCT	ENSP00000479931.1:n.457-282_457-281insCATCAGTTCT
NM_000136.2:c.457-282_457-281insCATCAGTTCT , LRG_497t1:c.457-282_457-281insCATCAGTTCT	NP_000127.2:n.457-282_457-281insCATCAGTTCT
NM_001243743.1:c.457-282_457-281insCATCAGTTCT	NP_001230672.1:n.457-282_457-281insCATCAGTTCT
NM_001243744.1:c.457-282_457-281insCATCAGTTCT	NP_001230673.1:n.457-282_457-281insCATCAGTTCT
XM_006717001.1:c.457-282_457-281insCATCAGTTCT	XP_006717064.1:n.457-282_457-281insCATCAGTTCT
XM_006717002.2:c.457-282_457-281insCATCAGTTCT	XP_006717065.1:n.457-282_457-281insCATCAGTTCT
XM_006717004.2:c.457-282_457-281insCATCAGTTCT	XP_006717067.1:n.457-282_457-281insCATCAGTTCT
XM_011518365.1:c.457-282_457-281insCATCAGTTCT	XP_011516667.1:n.457-282_457-281insCATCAGTTCT
XM_011518366.1:c.457-282_457-281insCATCAGTTCT	XP_011516668.1:n.457-282_457-281insCATCAGTTCT
XM_011518367.1:c.1-282_1-281insCATCAGTTCT	XP_011516669.1:n.1-282_1-281insCATCAGTTCT
XM_006717001.3:c.457-282_457-281insCATCAGTTCT	XP_006717064.1:n.457-282_457-281insCATCAGTTCT
XM_006717002.4:c.457-282_457-281insCATCAGTTCT	XP_006717065.1:n.457-282_457-281insCATCAGTTCT
XM_006717004.4:c.457-282_457-281insCATCAGTTCT	XP_006717067.1:n.457-282_457-281insCATCAGTTCT
XM_011518365.3:c.457-282_457-281insCATCAGTTCT	XP_011516667.1:n.457-282_457-281insCATCAGTTCT
XM_011518366.3:c.457-282_457-281insCATCAGTTCT	XP_011516668.1:n.457-282_457-281insCATCAGTTCT
XM_011518367.2:c.1-282_1-281insCATCAGTTCT	XP_011516669.1:n.1-282_1-281insCATCAGTTCT
XM_017014452.2:c.1-282_1-281insCATCAGTTCT	XP_016869941.1:n.1-282_1-281insCATCAGTTCT
XM_017014453.1:c.1-282_1-281insCATCAGTTCT	XP_016869942.1:n.1-282_1-281insCATCAGTTCT
XM_017014454.1:c.1-282_1-281insCATCAGTTCT	XP_016869943.1:n.1-282_1-281insCATCAGTTCT
XM_024447451.1:c.457-282_457-281insCATCAGTTCT	XP_024303219.1:n.457-282_457-281insCATCAGTTCT
NM_000136.3:c.457-282_457-281insCATCAGTTCT MANE Select	NP_000127.2:n.457-282_457-281insCATCAGTTCT
NM_001243743.2:c.457-282_457-281insCATCAGTTCT	NP_001230672.1:n.457-282_457-281insCATCAGTTCT
NM_001243744.2:c.457-282_457-281insCATCAGTTCT	NP_001230673.1:n.457-282_457-281insCATCAGTTCT