Canonical Allele Identifier: CA1865416343

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs2071928631

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111471_95111477del , CM000671.2:g.95111471_95111477del	GRCh38
NC_000009.11:g.97873753_97873759del , CM000671.1:g.97873753_97873759del	GRCh37
NC_000009.10:g.96913574_96913580del	NCBI36
NG_011707.1:g.211236_211242del , LRG_497:g.211236_211242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30691_410+30697del (AOPEP)
ENST00000696260.1:n.2133_2139del (FANCC)
ENST00000289081.8:c.1318_1324del (FANCC) MANE Select	ENSP00000289081.3:p.Ala440LeufsTer5
ENST00000375305.6:c.1318_1324del (FANCC)	ENSP00000364454.1:p.Ala440LeufsTer5
ENST00000490972.7:c.1318_1324del (FANCC)	ENSP00000479931.1:p.Ala440LeufsTer2
ENST00000649334.1:c.1463_1469del (FANCC)	ENSP00000497735.1:n.1463_1469del
ENST00000289081.7:c.1318_1324del (FANCC)	ENSP00000289081.3:p.Ala440LeufsTer5
ENST00000375305.5:c.1318_1324del (FANCC)	ENSP00000364454.1:p.Ala440LeufsTer5
ENST00000464627.5:n.645_651del (FANCC)
ENST00000477942.5:n.673_679del (FANCC)
ENST00000480712.5:n.503_509del (FANCC)
ENST00000490972.6:c.1318_1324del (FANCC)	ENSP00000479931.1:p.Ala440LeufsTer2
NM_000136.2:c.1318_1324del , LRG_497t1:c.1318_1324del (FANCC)	NP_000127.2:p.Ala440LeufsTer5
NM_001243743.1:c.1318_1324del (FANCC)	NP_001230672.1:p.Ala440LeufsTer5
NM_001243744.1:c.1318_1324del (FANCC)	NP_001230673.1:p.Ala440LeufsTer2
XM_005251802.2:c.637_643del (FANCC)	XP_005251859.1:p.Ala213LeufsTer5
XM_006717001.1:c.1153_1159del (FANCC)	XP_006717064.1:p.Ala385LeufsTer5
XM_006717002.2:c.1318_1324del (FANCC)	XP_006717065.1:p.Ala440LeufsTer10
XM_011518365.1:c.1318_1324del (FANCC)	XP_011516667.1:p.Ala440LeufsTer5
XM_011518366.1:c.1318_1324del (FANCC)	XP_011516668.1:p.Ala440LeufsTer?
XM_011518367.1:c.862_868del (FANCC)	XP_011516669.1:p.Ala288LeufsTer5
XM_011519121.1:c.2319+30691_2319+30697del (AOPEP)	XP_011517423.1:n.2319+30691_2319+30697del
XM_005251802.3:c.637_643del (FANCC)	XP_005251859.1:p.Ala213LeufsTer5
XM_006717001.3:c.1153_1159del (FANCC)	XP_006717064.1:p.Ala385LeufsTer5
XM_006717002.4:c.1318_1324del (FANCC)	XP_006717065.1:p.Ala440LeufsTer10
XM_011518365.3:c.1318_1324del (FANCC)	XP_011516667.1:p.Ala440LeufsTer5
XM_011518366.3:c.1318_1324del (FANCC)	XP_011516668.1:p.Ala440LeufsTer?
XM_011518367.2:c.862_868del (FANCC)	XP_011516669.1:p.Ala288LeufsTer5
XM_011519121.3:c.2319+30691_2319+30697del (AOPEP)	XP_011517423.1:n.2319+30691_2319+30697del
XM_017014452.2:c.862_868del (FANCC)	XP_016869941.1:p.Ala288LeufsTer5
XM_017014453.1:c.862_868del (FANCC)	XP_016869942.1:p.Ala288LeufsTer5
XM_017014454.1:c.697_703del (FANCC)	XP_016869943.1:p.Ala233LeufsTer5
XM_024447451.1:c.1318_1324del (FANCC)	XP_024303219.1:p.Ala440LeufsTer5
NM_000136.3:c.1318_1324del (FANCC) MANE Select	NP_000127.2:p.Ala440LeufsTer5
NM_001243743.2:c.1318_1324del (FANCC)	NP_001230672.1:p.Ala440LeufsTer5
NM_001243744.2:c.1318_1324del (FANCC)	NP_001230673.1:p.Ala440LeufsTer2