Canonical Allele Identifier: CA1865462016

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95106860_95106862delinsCCT , CM000671.2:g.95106860_95106862delinsCCT	GRCh38
NC_000009.11:g.97869142_97869144delinsCCT , CM000671.1:g.97869142_97869144delinsCCT	GRCh37
NC_000009.10:g.96908963_96908965delinsCCT	NCBI36
NG_011707.1:g.215848_215850delinsAGG , LRG_497:g.215848_215850delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26080_410+26082delinsCCT (AOPEP)
ENST00000696260.1:n.2348+204_2348+206delinsAGG (FANCC)
ENST00000289081.8:c.1533+204_1533+206delinsAGG (FANCC) MANE Select	ENSP00000289081.3:n.1533+204_1533+206delinsAGG
ENST00000375305.6:c.1533+204_1533+206delinsAGG (FANCC)	ENSP00000364454.1:n.1533+204_1533+206delinsAGG
ENST00000649334.1:c.1678+204_1678+206delinsAGG (FANCC)	ENSP00000497735.1:n.1678+204_1678+206delinsAGG
ENST00000289081.7:c.1533+204_1533+206delinsAGG (FANCC)	ENSP00000289081.3:n.1533+204_1533+206delinsAGG
ENST00000375305.5:c.1533+204_1533+206delinsAGG (FANCC)	ENSP00000364454.1:n.1533+204_1533+206delinsAGG
NM_000136.2:c.1533+204_1533+206delinsAGG , LRG_497t1:c.1533+204_1533+206delinsAGG (FANCC)	NP_000127.2:n.1533+204_1533+206delinsAGG
NM_001243743.1:c.1533+204_1533+206delinsAGG (FANCC)	NP_001230672.1:n.1533+204_1533+206delinsAGG
XM_005251802.2:c.852+204_852+206delinsAGG (FANCC)	XP_005251859.1:n.852+204_852+206delinsAGG
XM_006717001.1:c.1368+204_1368+206delinsAGG (FANCC)	XP_006717064.1:n.1368+204_1368+206delinsAGG
XM_011518365.1:c.1533+204_1533+206delinsAGG (FANCC)	XP_011516667.1:n.1533+204_1533+206delinsAGG
XM_011518367.1:c.1077+204_1077+206delinsAGG (FANCC)	XP_011516669.1:n.1077+204_1077+206delinsAGG
XM_011519121.1:c.2319+26080_2319+26082delinsCCT (AOPEP)	XP_011517423.1:n.2319+26080_2319+26082delinsCCT
XM_005251802.3:c.852+204_852+206delinsAGG (FANCC)	XP_005251859.1:n.852+204_852+206delinsAGG
XM_006717001.3:c.1368+204_1368+206delinsAGG (FANCC)	XP_006717064.1:n.1368+204_1368+206delinsAGG
XM_011518365.3:c.1533+204_1533+206delinsAGG (FANCC)	XP_011516667.1:n.1533+204_1533+206delinsAGG
XM_011518367.2:c.1077+204_1077+206delinsAGG (FANCC)	XP_011516669.1:n.1077+204_1077+206delinsAGG
XM_011519121.3:c.2319+26080_2319+26082delinsCCT (AOPEP)	XP_011517423.1:n.2319+26080_2319+26082delinsCCT
XM_017014452.2:c.1077+204_1077+206delinsAGG (FANCC)	XP_016869941.1:n.1077+204_1077+206delinsAGG
XM_017014453.1:c.1077+204_1077+206delinsAGG (FANCC)	XP_016869942.1:n.1077+204_1077+206delinsAGG
XM_017014454.1:c.912+204_912+206delinsAGG (FANCC)	XP_016869943.1:n.912+204_912+206delinsAGG
XM_024447451.1:c.1533+204_1533+206delinsAGG (FANCC)	XP_024303219.1:n.1533+204_1533+206delinsAGG
XR_001746847.1:n.306-28_306-26delinsCCT
NM_000136.3:c.1533+204_1533+206delinsAGG (FANCC) MANE Select	NP_000127.2:n.1533+204_1533+206delinsAGG
NM_001243743.2:c.1533+204_1533+206delinsAGG (FANCC)	NP_001230672.1:n.1533+204_1533+206delinsAGG