Canonical Allele Identifier: CA1865459603

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101891_95101895delinsCCAGA , CM000671.2:g.95101891_95101895delinsCCAGA	GRCh38
NC_000009.11:g.97864173_97864177delinsCCAGA , CM000671.1:g.97864173_97864177delinsCCAGA	GRCh37
NC_000009.10:g.96903994_96903998delinsCCAGA	NCBI36
NG_011707.1:g.220815_220819delinsTCTGG , LRG_497:g.220815_220819delinsTCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+21111_410+21115delinsCCAGA (AOPEP)
ENST00000696260.1:n.2349-45_2349-41delinsTCTGG (FANCC)
ENST00000289081.8:c.1534-45_1534-41delinsTCTGG (FANCC) MANE Select	ENSP00000289081.3:n.1534-45_1534-41delinsTCTGG
ENST00000375305.6:c.1534-45_1534-41delinsTCTGG (FANCC)	ENSP00000364454.1:n.1534-45_1534-41delinsTCTGG
ENST00000649334.1:c.1679-45_1679-41delinsTCTGG (FANCC)	ENSP00000497735.1:n.1679-45_1679-41delinsTCTGG
ENST00000289081.7:c.1534-45_1534-41delinsTCTGG (FANCC)	ENSP00000289081.3:n.1534-45_1534-41delinsTCTGG
ENST00000375305.5:c.1534-45_1534-41delinsTCTGG (FANCC)	ENSP00000364454.1:n.1534-45_1534-41delinsTCTGG
NM_000136.2:c.1534-45_1534-41delinsTCTGG , LRG_497t1:c.1534-45_1534-41delinsTCTGG (FANCC)	NP_000127.2:n.1534-45_1534-41delinsTCTGG
NM_001243743.1:c.1534-45_1534-41delinsTCTGG (FANCC)	NP_001230672.1:n.1534-45_1534-41delinsTCTGG
XM_005251802.2:c.853-45_853-41delinsTCTGG (FANCC)	XP_005251859.1:n.853-45_853-41delinsTCTGG
XM_006717001.1:c.1369-45_1369-41delinsTCTGG (FANCC)	XP_006717064.1:n.1369-45_1369-41delinsTCTGG
XM_011518365.1:c.1534-45_1534-41delinsTCTGG (FANCC)	XP_011516667.1:n.1534-45_1534-41delinsTCTGG
XM_011518367.1:c.1078-45_1078-41delinsTCTGG (FANCC)	XP_011516669.1:n.1078-45_1078-41delinsTCTGG
XM_011519121.1:c.2319+21111_2319+21115delinsCCAGA (AOPEP)	XP_011517423.1:n.2319+21111_2319+21115delinsCCAGA
XM_005251802.3:c.853-45_853-41delinsTCTGG (FANCC)	XP_005251859.1:n.853-45_853-41delinsTCTGG
XM_006717001.3:c.1369-45_1369-41delinsTCTGG (FANCC)	XP_006717064.1:n.1369-45_1369-41delinsTCTGG
XM_011518365.3:c.1534-45_1534-41delinsTCTGG (FANCC)	XP_011516667.1:n.1534-45_1534-41delinsTCTGG
XM_011518367.2:c.1078-45_1078-41delinsTCTGG (FANCC)	XP_011516669.1:n.1078-45_1078-41delinsTCTGG
XM_011519121.3:c.2319+21111_2319+21115delinsCCAGA (AOPEP)	XP_011517423.1:n.2319+21111_2319+21115delinsCCAGA
XM_017014452.2:c.1078-45_1078-41delinsTCTGG (FANCC)	XP_016869941.1:n.1078-45_1078-41delinsTCTGG
XM_017014453.1:c.1078-45_1078-41delinsTCTGG (FANCC)	XP_016869942.1:n.1078-45_1078-41delinsTCTGG
XM_017014454.1:c.913-45_913-41delinsTCTGG (FANCC)	XP_016869943.1:n.913-45_913-41delinsTCTGG
XM_024447451.1:c.1534-45_1534-41delinsTCTGG (FANCC)	XP_024303219.1:n.1534-45_1534-41delinsTCTGG
NM_000136.3:c.1534-45_1534-41delinsTCTGG (FANCC) MANE Select	NP_000127.2:n.1534-45_1534-41delinsTCTGG
NM_001243743.2:c.1534-45_1534-41delinsTCTGG (FANCC)	NP_001230672.1:n.1534-45_1534-41delinsTCTGG