Canonical Allele Identifier: CA1865419418

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95114519A= , CM000671.2:g.95114519A=	GRCh38
NC_000009.11:g.97876801A= , CM000671.1:g.97876801A=	GRCh37
NC_000009.10:g.96916622A=	NCBI36
NG_011707.1:g.208191T= , LRG_497:g.208191T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-32692A= (AOPEP)
ENST00000289081.8:c.1154+110T= (FANCC) MANE Select	ENSP00000289081.3:n.1154+110T=
ENST00000375305.6:c.1154+110T= (FANCC)	ENSP00000364454.1:n.1154+110T=
ENST00000490972.7:c.1154+110T= (FANCC)	ENSP00000479931.1:n.1154+110T=
ENST00000649334.1:c.1299+110T= (FANCC)	ENSP00000497735.1:n.1299+110T=
ENST00000289081.7:c.1154+110T= (FANCC)	ENSP00000289081.3:n.1154+110T=
ENST00000375305.5:c.1154+110T= (FANCC)	ENSP00000364454.1:n.1154+110T=
ENST00000464627.5:n.481+110T= (FANCC)
ENST00000464653.1:n.1260T= (FANCC)
ENST00000477942.5:n.509+110T= (FANCC)
ENST00000480712.5:n.339+110T= (FANCC)
ENST00000490972.6:c.1154+110T= (FANCC)	ENSP00000479931.1:n.1154+110T=
NM_000136.2:c.1154+110T= , LRG_497t1:c.1154+110T= (FANCC)	NP_000127.2:n.1154+110T=
NM_001243743.1:c.1154+110T= (FANCC)	NP_001230672.1:n.1154+110T=
NM_001243744.1:c.1154+110T= (FANCC)	NP_001230673.1:n.1154+110T=
XM_005251802.2:c.473+110T= (FANCC)	XP_005251859.1:n.473+110T=
XM_006717001.1:c.989+110T= (FANCC)	XP_006717064.1:n.989+110T=
XM_006717002.2:c.1154+110T= (FANCC)	XP_006717065.1:n.1154+110T=
XM_006717004.2:c.*49+110T= (FANCC)	XP_006717067.1:n.*49+110T=
XM_011518365.1:c.1154+110T= (FANCC)	XP_011516667.1:n.1154+110T=
XM_011518366.1:c.1154+110T= (FANCC)	XP_011516668.1:n.1154+110T=
XM_011518367.1:c.698+110T= (FANCC)	XP_011516669.1:n.698+110T=
XM_011519121.1:c.2320-32692A= (AOPEP)	XP_011517423.1:n.2320-32692A=
XM_005251802.3:c.473+110T= (FANCC)	XP_005251859.1:n.473+110T=
XM_006717001.3:c.989+110T= (FANCC)	XP_006717064.1:n.989+110T=
XM_006717002.4:c.1154+110T= (FANCC)	XP_006717065.1:n.1154+110T=
XM_006717004.4:c.*49+110T= (FANCC)	XP_006717067.1:n.*49+110T=
XM_011518365.3:c.1154+110T= (FANCC)	XP_011516667.1:n.1154+110T=
XM_011518366.3:c.1154+110T= (FANCC)	XP_011516668.1:n.1154+110T=
XM_011518367.2:c.698+110T= (FANCC)	XP_011516669.1:n.698+110T=
XM_011519121.3:c.2320-32692A= (AOPEP)	XP_011517423.1:n.2320-32692A=
XM_017014452.2:c.698+110T= (FANCC)	XP_016869941.1:n.698+110T=
XM_017014453.1:c.698+110T= (FANCC)	XP_016869942.1:n.698+110T=
XM_017014454.1:c.533+110T= (FANCC)	XP_016869943.1:n.533+110T=
XM_024447451.1:c.1154+110T= (FANCC)	XP_024303219.1:n.1154+110T=
NM_000136.3:c.1154+110T= (FANCC) MANE Select	NP_000127.2:n.1154+110T=
NM_001243743.2:c.1154+110T= (FANCC)	NP_001230672.1:n.1154+110T=
NM_001243744.2:c.1154+110T= (FANCC)	NP_001230673.1:n.1154+110T=