Canonical Allele Identifier: CA1865416344

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111469_95111471delinsCTG , CM000671.2:g.95111469_95111471delinsCTG	GRCh38
NC_000009.11:g.97873751_97873753delinsCTG , CM000671.1:g.97873751_97873753delinsCTG	GRCh37
NC_000009.10:g.96913572_96913574delinsCTG	NCBI36
NG_011707.1:g.211239_211241delinsCAG , LRG_497:g.211239_211241delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30689_410+30691delinsCTG (AOPEP)
ENST00000696260.1:n.2136_2138delinsCAG (FANCC)
ENST00000289081.8:c.1321_1323delinsCAG (FANCC) MANE Select	ENSP00000289081.3:p.Gln441=
ENST00000375305.6:c.1321_1323delinsCAG (FANCC)	ENSP00000364454.1:p.Gln441=
ENST00000490972.7:c.1321_1323delinsCAG (FANCC)	ENSP00000479931.1:p.Gln441=
ENST00000649334.1:c.1466_1468delinsCAG (FANCC)	ENSP00000497735.1:n.1466_1468delinsCAG
ENST00000289081.7:c.1321_1323delinsCAG (FANCC)	ENSP00000289081.3:p.Gln441=
ENST00000375305.5:c.1321_1323delinsCAG (FANCC)	ENSP00000364454.1:p.Gln441=
ENST00000464627.5:n.648_650delinsCAG (FANCC)
ENST00000477942.5:n.676_678delinsCAG (FANCC)
ENST00000480712.5:n.506_508delinsCAG (FANCC)
ENST00000490972.6:c.1321_1323delinsCAG (FANCC)	ENSP00000479931.1:p.Gln441=
NM_000136.2:c.1321_1323delinsCAG , LRG_497t1:c.1321_1323delinsCAG (FANCC)	NP_000127.2:p.Gln441=
NM_001243743.1:c.1321_1323delinsCAG (FANCC)	NP_001230672.1:p.Gln441=
NM_001243744.1:c.1321_1323delinsCAG (FANCC)	NP_001230673.1:p.Gln441=
XM_005251802.2:c.640_642delinsCAG (FANCC)	XP_005251859.1:p.Gln214=
XM_006717001.1:c.1156_1158delinsCAG (FANCC)	XP_006717064.1:p.Gln386=
XM_006717002.2:c.1321_1323delinsCAG (FANCC)	XP_006717065.1:p.Gln441=
XM_011518365.1:c.1321_1323delinsCAG (FANCC)	XP_011516667.1:p.Gln441=
XM_011518366.1:c.1321_1323delinsCAG (FANCC)	XP_011516668.1:p.Gln441=
XM_011518367.1:c.865_867delinsCAG (FANCC)	XP_011516669.1:p.Gln289=
XM_011519121.1:c.2319+30689_2319+30691delinsCTG (AOPEP)	XP_011517423.1:n.2319+30689_2319+30691delinsCTG
XM_005251802.3:c.640_642delinsCAG (FANCC)	XP_005251859.1:p.Gln214=
XM_006717001.3:c.1156_1158delinsCAG (FANCC)	XP_006717064.1:p.Gln386=
XM_006717002.4:c.1321_1323delinsCAG (FANCC)	XP_006717065.1:p.Gln441=
XM_011518365.3:c.1321_1323delinsCAG (FANCC)	XP_011516667.1:p.Gln441=
XM_011518366.3:c.1321_1323delinsCAG (FANCC)	XP_011516668.1:p.Gln441=
XM_011518367.2:c.865_867delinsCAG (FANCC)	XP_011516669.1:p.Gln289=
XM_011519121.3:c.2319+30689_2319+30691delinsCTG (AOPEP)	XP_011517423.1:n.2319+30689_2319+30691delinsCTG
XM_017014452.2:c.865_867delinsCAG (FANCC)	XP_016869941.1:p.Gln289=
XM_017014453.1:c.865_867delinsCAG (FANCC)	XP_016869942.1:p.Gln289=
XM_017014454.1:c.700_702delinsCAG (FANCC)	XP_016869943.1:p.Gln234=
XM_024447451.1:c.1321_1323delinsCAG (FANCC)	XP_024303219.1:p.Gln441=
NM_000136.3:c.1321_1323delinsCAG (FANCC) MANE Select	NP_000127.2:p.Gln441=
NM_001243743.2:c.1321_1323delinsCAG (FANCC)	NP_001230672.1:p.Gln441=
NM_001243744.2:c.1321_1323delinsCAG (FANCC)	NP_001230673.1:p.Gln441=