Canonical Allele Identifier: CA1865483104

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171104_95171106delinsGAT , CM000671.2:g.95171104_95171106delinsGAT	GRCh38
NC_000009.11:g.97933386_97933388delinsGAT , CM000671.1:g.97933386_97933388delinsGAT	GRCh37
NC_000009.10:g.96973207_96973209delinsGAT	NCBI36
NG_011707.1:g.151604_151606delinsATC , LRG_497:g.151604_151606delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.885_887delinsATC
ENST00000289081.8:c.494_496delinsATC MANE Select	ENSP00000289081.3:p.His165=
ENST00000375305.6:c.494_496delinsATC	ENSP00000364454.1:p.His165=
ENST00000490972.7:c.494_496delinsATC	ENSP00000479931.1:p.His165=
ENST00000636777.1:n.552_554delinsATC
ENST00000649334.1:c.639_641delinsATC	ENSP00000497735.1:n.639_641delinsATC
ENST00000649701.1:n.209_211delinsATC
ENST00000289081.7:c.494_496delinsATC	ENSP00000289081.3:p.His165=
ENST00000375305.5:c.494_496delinsATC	ENSP00000364454.1:p.His165=
ENST00000490972.6:c.494_496delinsATC	ENSP00000479931.1:p.His165=
NM_000136.2:c.494_496delinsATC , LRG_497t1:c.494_496delinsATC	NP_000127.2:p.His165=
NM_001243743.1:c.494_496delinsATC	NP_001230672.1:p.His165=
NM_001243744.1:c.494_496delinsATC	NP_001230673.1:p.His165=
XM_006717001.1:c.494_496delinsATC	XP_006717064.1:p.His165=
XM_006717002.2:c.494_496delinsATC	XP_006717065.1:p.His165=
XM_006717004.2:c.494_496delinsATC	XP_006717067.1:p.His165=
XM_011518365.1:c.494_496delinsATC	XP_011516667.1:p.His165=
XM_011518366.1:c.494_496delinsATC	XP_011516668.1:p.His165=
XM_011518367.1:c.38_40delinsATC	XP_011516669.1:p.His13=
XM_006717001.3:c.494_496delinsATC	XP_006717064.1:p.His165=
XM_006717002.4:c.494_496delinsATC	XP_006717065.1:p.His165=
XM_006717004.4:c.494_496delinsATC	XP_006717067.1:p.His165=
XM_011518365.3:c.494_496delinsATC	XP_011516667.1:p.His165=
XM_011518366.3:c.494_496delinsATC	XP_011516668.1:p.His165=
XM_011518367.2:c.38_40delinsATC	XP_011516669.1:p.His13=
XM_017014452.2:c.38_40delinsATC	XP_016869941.1:p.His13=
XM_017014453.1:c.38_40delinsATC	XP_016869942.1:p.His13=
XM_017014454.1:c.38_40delinsATC	XP_016869943.1:p.His13=
XM_024447451.1:c.494_496delinsATC	XP_024303219.1:p.His165=
NM_000136.3:c.494_496delinsATC MANE Select	NP_000127.2:p.His165=
NM_001243743.2:c.494_496delinsATC	NP_001230672.1:p.His165=
NM_001243744.2:c.494_496delinsATC	NP_001230673.1:p.His165=