Canonical Allele Identifier: CA1865462113

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107070G= , CM000671.2:g.95107070G=	GRCh38
NC_000009.11:g.97869352G= , CM000671.1:g.97869352G=	GRCh37
NC_000009.10:g.96909173G=	NCBI36
NG_011707.1:g.215640C= , LRG_497:g.215640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26290G= (AOPEP)
ENST00000696260.1:n.2344C= (FANCC)
ENST00000289081.8:c.1529C= (FANCC) MANE Select	ENSP00000289081.3:p.Thr510=
ENST00000375305.6:c.1529C= (FANCC)	ENSP00000364454.1:p.Thr510=
ENST00000649334.1:c.1674C= (FANCC)	ENSP00000497735.1:n.1674C=
ENST00000289081.7:c.1529C= (FANCC)	ENSP00000289081.3:p.Thr510=
ENST00000375305.5:c.1529C= (FANCC)	ENSP00000364454.1:p.Thr510=
NM_000136.2:c.1529C= , LRG_497t1:c.1529C= (FANCC)	NP_000127.2:p.Thr510=
NM_001243743.1:c.1529C= (FANCC)	NP_001230672.1:p.Thr510=
XM_005251802.2:c.848C= (FANCC)	XP_005251859.1:p.Thr283=
XM_006717001.1:c.1364C= (FANCC)	XP_006717064.1:p.Thr455=
XM_011518365.1:c.1529C= (FANCC)	XP_011516667.1:p.Thr510=
XM_011518367.1:c.1073C= (FANCC)	XP_011516669.1:p.Thr358=
XM_011519121.1:c.2319+26290G= (AOPEP)	XP_011517423.1:n.2319+26290G=
XM_005251802.3:c.848C= (FANCC)	XP_005251859.1:p.Thr283=
XM_006717001.3:c.1364C= (FANCC)	XP_006717064.1:p.Thr455=
XM_011518365.3:c.1529C= (FANCC)	XP_011516667.1:p.Thr510=
XM_011518367.2:c.1073C= (FANCC)	XP_011516669.1:p.Thr358=
XM_011519121.3:c.2319+26290G= (AOPEP)	XP_011517423.1:n.2319+26290G=
XM_017014452.2:c.1073C= (FANCC)	XP_016869941.1:p.Thr358=
XM_017014453.1:c.1073C= (FANCC)	XP_016869942.1:p.Thr358=
XM_017014454.1:c.908C= (FANCC)	XP_016869943.1:p.Thr303=
XM_024447451.1:c.1529C= (FANCC)	XP_024303219.1:p.Thr510=
XR_001746847.1:n.488G=
NM_000136.3:c.1529C= (FANCC) MANE Select	NP_000127.2:p.Thr510=
NM_001243743.2:c.1529C= (FANCC)	NP_001230672.1:p.Thr510=