Canonical Allele Identifier: CA2580080685

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 2116750
• ClinVar RCV Id: RCV003027395

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95114620T>C , CM000671.2:g.95114620T>C	GRCh38
NC_000009.11:g.97876902T>C , CM000671.1:g.97876902T>C	GRCh37
NC_000009.10:g.96916723T>C	NCBI36
NG_011707.1:g.208090A>G , LRG_497:g.208090A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-32591T>C (AOPEP)
ENST00000289081.8:c.1154+9A>G (FANCC) MANE Select	ENSP00000289081.3:n.1154+9A>G
ENST00000375305.6:c.1154+9A>G (FANCC)	ENSP00000364454.1:n.1154+9A>G
ENST00000490972.7:c.1154+9A>G (FANCC)	ENSP00000479931.1:n.1154+9A>G
ENST00000649334.1:c.1299+9A>G (FANCC)	ENSP00000497735.1:n.1299+9A>G
ENST00000289081.7:c.1154+9A>G (FANCC)	ENSP00000289081.3:n.1154+9A>G
ENST00000375305.5:c.1154+9A>G (FANCC)	ENSP00000364454.1:n.1154+9A>G
ENST00000464627.5:n.481+9A>G (FANCC)
ENST00000464653.1:n.1159A>G (FANCC)
ENST00000477942.5:n.509+9A>G (FANCC)
ENST00000480712.5:n.339+9A>G (FANCC)
ENST00000490972.6:c.1154+9A>G (FANCC)	ENSP00000479931.1:n.1154+9A>G
NM_000136.2:c.1154+9A>G , LRG_497t1:c.1154+9A>G (FANCC)	NP_000127.2:n.1154+9A>G
NM_001243743.1:c.1154+9A>G (FANCC)	NP_001230672.1:n.1154+9A>G
NM_001243744.1:c.1154+9A>G (FANCC)	NP_001230673.1:n.1154+9A>G
XM_005251802.2:c.473+9A>G (FANCC)	XP_005251859.1:n.473+9A>G
XM_006717001.1:c.989+9A>G (FANCC)	XP_006717064.1:n.989+9A>G
XM_006717002.2:c.1154+9A>G (FANCC)	XP_006717065.1:n.1154+9A>G
XM_006717004.2:c.*49+9A>G (FANCC)	XP_006717067.1:n.*49+9A>G
XM_011518365.1:c.1154+9A>G (FANCC)	XP_011516667.1:n.1154+9A>G
XM_011518366.1:c.1154+9A>G (FANCC)	XP_011516668.1:n.1154+9A>G
XM_011518367.1:c.698+9A>G (FANCC)	XP_011516669.1:n.698+9A>G
XM_011519121.1:c.2320-32591T>C (AOPEP)	XP_011517423.1:n.2320-32591T>C
XM_005251802.3:c.473+9A>G (FANCC)	XP_005251859.1:n.473+9A>G
XM_006717001.3:c.989+9A>G (FANCC)	XP_006717064.1:n.989+9A>G
XM_006717002.4:c.1154+9A>G (FANCC)	XP_006717065.1:n.1154+9A>G
XM_006717004.4:c.*49+9A>G (FANCC)	XP_006717067.1:n.*49+9A>G
XM_011518365.3:c.1154+9A>G (FANCC)	XP_011516667.1:n.1154+9A>G
XM_011518366.3:c.1154+9A>G (FANCC)	XP_011516668.1:n.1154+9A>G
XM_011518367.2:c.698+9A>G (FANCC)	XP_011516669.1:n.698+9A>G
XM_011519121.3:c.2320-32591T>C (AOPEP)	XP_011517423.1:n.2320-32591T>C
XM_017014452.2:c.698+9A>G (FANCC)	XP_016869941.1:n.698+9A>G
XM_017014453.1:c.698+9A>G (FANCC)	XP_016869942.1:n.698+9A>G
XM_017014454.1:c.533+9A>G (FANCC)	XP_016869943.1:n.533+9A>G
XM_024447451.1:c.1154+9A>G (FANCC)	XP_024303219.1:n.1154+9A>G
NM_000136.3:c.1154+9A>G (FANCC) MANE Select	NP_000127.2:n.1154+9A>G
NM_001243743.2:c.1154+9A>G (FANCC)	NP_001230672.1:n.1154+9A>G
NM_001243744.2:c.1154+9A>G (FANCC)	NP_001230673.1:n.1154+9A>G