Canonical Allele Identifier: CA1865438187

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135404A= , CM000671.2:g.95135404A=	GRCh38
NC_000009.11:g.97897686A= , CM000671.1:g.97897686A=	GRCh37
NC_000009.10:g.96937507A=	NCBI36
NG_011707.1:g.187306T= , LRG_497:g.187306T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-11807A= (AOPEP)
ENST00000696261.1:n.1176T= (FANCC)
ENST00000289081.8:c.785T= (FANCC) MANE Select	ENSP00000289081.3:p.Ile262=
ENST00000375305.6:c.785T= (FANCC)	ENSP00000364454.1:p.Ile262=
ENST00000490972.7:c.785T= (FANCC)	ENSP00000479931.1:p.Ile262=
ENST00000649334.1:c.930T= (FANCC)	ENSP00000497735.1:n.930T=
ENST00000649701.1:n.500T= (FANCC)
ENST00000289081.7:c.785T= (FANCC)	ENSP00000289081.3:p.Ile262=
ENST00000375305.5:c.785T= (FANCC)	ENSP00000364454.1:p.Ile262=
ENST00000477942.5:n.140T= (FANCC)
ENST00000490972.6:c.785T= (FANCC)	ENSP00000479931.1:p.Ile262=
NM_000136.2:c.785T= , LRG_497t1:c.785T= (FANCC)	NP_000127.2:p.Ile262=
NM_001243743.1:c.785T= (FANCC)	NP_001230672.1:p.Ile262=
NM_001243744.1:c.785T= (FANCC)	NP_001230673.1:p.Ile262=
XM_005251802.2:c.104T= (FANCC)	XP_005251859.1:p.Ile35=
XM_006717001.1:c.620T= (FANCC)	XP_006717064.1:p.Ile207=
XM_006717002.2:c.785T= (FANCC)	XP_006717065.1:p.Ile262=
XM_006717004.2:c.785T= (FANCC)	XP_006717067.1:p.Ile262=
XM_011518365.1:c.785T= (FANCC)	XP_011516667.1:p.Ile262=
XM_011518366.1:c.785T= (FANCC)	XP_011516668.1:p.Ile262=
XM_011518367.1:c.329T= (FANCC)	XP_011516669.1:p.Ile110=
XM_011519121.1:c.2320-11807A= (AOPEP)	XP_011517423.1:n.2320-11807A=
XM_005251802.3:c.104T= (FANCC)	XP_005251859.1:p.Ile35=
XM_006717001.3:c.620T= (FANCC)	XP_006717064.1:p.Ile207=
XM_006717002.4:c.785T= (FANCC)	XP_006717065.1:p.Ile262=
XM_006717004.4:c.785T= (FANCC)	XP_006717067.1:p.Ile262=
XM_011518365.3:c.785T= (FANCC)	XP_011516667.1:p.Ile262=
XM_011518366.3:c.785T= (FANCC)	XP_011516668.1:p.Ile262=
XM_011518367.2:c.329T= (FANCC)	XP_011516669.1:p.Ile110=
XM_011519121.3:c.2320-11807A= (AOPEP)	XP_011517423.1:n.2320-11807A=
XM_017014452.2:c.329T= (FANCC)	XP_016869941.1:p.Ile110=
XM_017014453.1:c.329T= (FANCC)	XP_016869942.1:p.Ile110=
XM_017014454.1:c.164T= (FANCC)	XP_016869943.1:p.Ile55=
XM_024447451.1:c.785T= (FANCC)	XP_024303219.1:p.Ile262=
NM_000136.3:c.785T= (FANCC) MANE Select	NP_000127.2:p.Ile262=
NM_001243743.2:c.785T= (FANCC)	NP_001230672.1:p.Ile262=
NM_001243744.2:c.785T= (FANCC)	NP_001230673.1:p.Ile262=