Canonical Allele Identifier: CA1865438202

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135419A= , CM000671.2:g.95135419A=	GRCh38
NC_000009.11:g.97897701A= , CM000671.1:g.97897701A=	GRCh37
NC_000009.10:g.96937522A=	NCBI36
NG_011707.1:g.187291T= , LRG_497:g.187291T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-11792A= (AOPEP)
ENST00000696261.1:n.1161T= (FANCC)
ENST00000289081.8:c.770T= (FANCC) MANE Select	ENSP00000289081.3:p.Leu257=
ENST00000375305.6:c.770T= (FANCC)	ENSP00000364454.1:p.Leu257=
ENST00000490972.7:c.770T= (FANCC)	ENSP00000479931.1:p.Leu257=
ENST00000649334.1:c.915T= (FANCC)	ENSP00000497735.1:n.915T=
ENST00000649701.1:n.485T= (FANCC)
ENST00000289081.7:c.770T= (FANCC)	ENSP00000289081.3:p.Leu257=
ENST00000375305.5:c.770T= (FANCC)	ENSP00000364454.1:p.Leu257=
ENST00000477942.5:n.125T= (FANCC)
ENST00000490972.6:c.770T= (FANCC)	ENSP00000479931.1:p.Leu257=
NM_000136.2:c.770T= , LRG_497t1:c.770T= (FANCC)	NP_000127.2:p.Leu257=
NM_001243743.1:c.770T= (FANCC)	NP_001230672.1:p.Leu257=
NM_001243744.1:c.770T= (FANCC)	NP_001230673.1:p.Leu257=
XM_005251802.2:c.89T= (FANCC)	XP_005251859.1:p.Leu30=
XM_006717001.1:c.605T= (FANCC)	XP_006717064.1:p.Leu202=
XM_006717002.2:c.770T= (FANCC)	XP_006717065.1:p.Leu257=
XM_006717004.2:c.770T= (FANCC)	XP_006717067.1:p.Leu257=
XM_011518365.1:c.770T= (FANCC)	XP_011516667.1:p.Leu257=
XM_011518366.1:c.770T= (FANCC)	XP_011516668.1:p.Leu257=
XM_011518367.1:c.314T= (FANCC)	XP_011516669.1:p.Leu105=
XM_011519121.1:c.2320-11792A= (AOPEP)	XP_011517423.1:n.2320-11792A=
XM_005251802.3:c.89T= (FANCC)	XP_005251859.1:p.Leu30=
XM_006717001.3:c.605T= (FANCC)	XP_006717064.1:p.Leu202=
XM_006717002.4:c.770T= (FANCC)	XP_006717065.1:p.Leu257=
XM_006717004.4:c.770T= (FANCC)	XP_006717067.1:p.Leu257=
XM_011518365.3:c.770T= (FANCC)	XP_011516667.1:p.Leu257=
XM_011518366.3:c.770T= (FANCC)	XP_011516668.1:p.Leu257=
XM_011518367.2:c.314T= (FANCC)	XP_011516669.1:p.Leu105=
XM_011519121.3:c.2320-11792A= (AOPEP)	XP_011517423.1:n.2320-11792A=
XM_017014452.2:c.314T= (FANCC)	XP_016869941.1:p.Leu105=
XM_017014453.1:c.314T= (FANCC)	XP_016869942.1:p.Leu105=
XM_017014454.1:c.149T= (FANCC)	XP_016869943.1:p.Leu50=
XM_024447451.1:c.770T= (FANCC)	XP_024303219.1:p.Leu257=
NM_000136.3:c.770T= (FANCC) MANE Select	NP_000127.2:p.Leu257=
NM_001243743.2:c.770T= (FANCC)	NP_001230672.1:p.Leu257=
NM_001243744.2:c.770T= (FANCC)	NP_001230673.1:p.Leu257=