Canonical Allele Identifier: CA466351565

Gene: AOPEP FANCC

Linked Data

• MyVariant Identifiers: chr9:g.97873868T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111586T>C , CM000671.2:g.95111586T>C	GRCh38
NC_000009.11:g.97873868T>C , CM000671.1:g.97873868T>C	GRCh37
NC_000009.10:g.96913689T>C	NCBI36
NG_011707.1:g.211124A>G , LRG_497:g.211124A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30806T>C (AOPEP)
ENST00000696260.1:n.2021A>G (FANCC)
ENST00000289081.8:c.1206A>G (FANCC) MANE Select	ENSP00000289081.3:p.Gly402=
ENST00000375305.6:c.1206A>G (FANCC)	ENSP00000364454.1:p.Gly402=
ENST00000490972.7:c.1206A>G (FANCC)	ENSP00000479931.1:p.Gly402=
ENST00000649334.1:c.1351A>G (FANCC)	ENSP00000497735.1:n.1351A>G
ENST00000289081.7:c.1206A>G (FANCC)	ENSP00000289081.3:p.Gly402=
ENST00000375305.5:c.1206A>G (FANCC)	ENSP00000364454.1:p.Gly402=
ENST00000464627.5:n.533A>G (FANCC)
ENST00000477942.5:n.561A>G (FANCC)
ENST00000480712.5:n.391A>G (FANCC)
ENST00000490972.6:c.1206A>G (FANCC)	ENSP00000479931.1:p.Gly402=
NM_000136.2:c.1206A>G , LRG_497t1:c.1206A>G (FANCC)	NP_000127.2:p.Gly402=
NM_001243743.1:c.1206A>G (FANCC)	NP_001230672.1:p.Gly402=
NM_001243744.1:c.1206A>G (FANCC)	NP_001230673.1:p.Gly402=
XM_005251802.2:c.525A>G (FANCC)	XP_005251859.1:p.Gly175=
XM_006717001.1:c.1041A>G (FANCC)	XP_006717064.1:p.Gly347=
XM_006717002.2:c.1206A>G (FANCC)	XP_006717065.1:p.Gly402=
XM_006717004.2:c.*101A>G (FANCC)	XP_006717067.1:n.*101A>G
XM_011518365.1:c.1206A>G (FANCC)	XP_011516667.1:p.Gly402=
XM_011518366.1:c.1206A>G (FANCC)	XP_011516668.1:p.Gly402=
XM_011518367.1:c.750A>G (FANCC)	XP_011516669.1:p.Gly250=
XM_011519121.1:c.2319+30806T>C (AOPEP)	XP_011517423.1:n.2319+30806T>C
XM_005251802.3:c.525A>G (FANCC)	XP_005251859.1:p.Gly175=
XM_006717001.3:c.1041A>G (FANCC)	XP_006717064.1:p.Gly347=
XM_006717002.4:c.1206A>G (FANCC)	XP_006717065.1:p.Gly402=
XM_006717004.4:c.*101A>G (FANCC)	XP_006717067.1:n.*101A>G
XM_011518365.3:c.1206A>G (FANCC)	XP_011516667.1:p.Gly402=
XM_011518366.3:c.1206A>G (FANCC)	XP_011516668.1:p.Gly402=
XM_011518367.2:c.750A>G (FANCC)	XP_011516669.1:p.Gly250=
XM_011519121.3:c.2319+30806T>C (AOPEP)	XP_011517423.1:n.2319+30806T>C
XM_017014452.2:c.750A>G (FANCC)	XP_016869941.1:p.Gly250=
XM_017014453.1:c.750A>G (FANCC)	XP_016869942.1:p.Gly250=
XM_017014454.1:c.585A>G (FANCC)	XP_016869943.1:p.Gly195=
XM_024447451.1:c.1206A>G (FANCC)	XP_024303219.1:p.Gly402=
NM_000136.3:c.1206A>G (FANCC) MANE Select	NP_000127.2:p.Gly402=
NM_001243743.2:c.1206A>G (FANCC)	NP_001230672.1:p.Gly402=
NM_001243744.2:c.1206A>G (FANCC)	NP_001230673.1:p.Gly402=