Canonical Allele Identifier: CA653183364

Gene: AOPEP FANCC

Linked Data

• gnomAD v4: 9-95135224-TTA-T
• COSMIC: COSN15649299

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135231_95135232del , CM000671.2:g.95135231_95135232del	GRCh38
NC_000009.11:g.97897513_97897514del , CM000671.1:g.97897513_97897514del	GRCh37
NC_000009.10:g.96937334_96937335del	NCBI36
NG_011707.1:g.187484_187485del , LRG_497:g.187484_187485del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.411-11980_411-11979del (AOPEP)
ENST00000696261.1:n.1354_1355del (FANCC)
ENST00000289081.8:c.843+120_843+121del (FANCC) MANE Select	ENSP00000289081.3:n.843+120_843+121del
ENST00000375305.6:c.843+120_843+121del (FANCC)	ENSP00000364454.1:n.843+120_843+121del
ENST00000490972.7:c.843+120_843+121del (FANCC)	ENSP00000479931.1:n.843+120_843+121del
ENST00000649334.1:c.988+120_988+121del (FANCC)	ENSP00000497735.1:n.988+120_988+121del
ENST00000649701.1:n.558+120_558+121del (FANCC)
ENST00000289081.7:c.843+120_843+121del (FANCC)	ENSP00000289081.3:n.843+120_843+121del
ENST00000375305.5:c.843+120_843+121del (FANCC)	ENSP00000364454.1:n.843+120_843+121del
ENST00000477942.5:n.198+120_198+121del (FANCC)
ENST00000480712.5:n.28+120_28+121del (FANCC)
ENST00000490972.6:c.843+120_843+121del (FANCC)	ENSP00000479931.1:n.843+120_843+121del
NM_000136.2:c.843+120_843+121del , LRG_497t1:c.843+120_843+121del (FANCC)	NP_000127.2:n.843+120_843+121del
NM_001243743.1:c.843+120_843+121del (FANCC)	NP_001230672.1:n.843+120_843+121del
NM_001243744.1:c.843+120_843+121del (FANCC)	NP_001230673.1:n.843+120_843+121del
XM_005251802.2:c.162+120_162+121del (FANCC)	XP_005251859.1:n.162+120_162+121del
XM_006717001.1:c.678+120_678+121del (FANCC)	XP_006717064.1:n.678+120_678+121del
XM_006717002.2:c.843+120_843+121del (FANCC)	XP_006717065.1:n.843+120_843+121del
XM_006717004.2:c.843+120_843+121del (FANCC)	XP_006717067.1:n.843+120_843+121del
XM_011518365.1:c.843+120_843+121del (FANCC)	XP_011516667.1:n.843+120_843+121del
XM_011518366.1:c.843+120_843+121del (FANCC)	XP_011516668.1:n.843+120_843+121del
XM_011518367.1:c.387+120_387+121del (FANCC)	XP_011516669.1:n.387+120_387+121del
XM_011519121.1:c.2320-11980_2320-11979del (AOPEP)	XP_011517423.1:n.2320-11980_2320-11979del
XM_005251802.3:c.162+120_162+121del (FANCC)	XP_005251859.1:n.162+120_162+121del
XM_006717001.3:c.678+120_678+121del (FANCC)	XP_006717064.1:n.678+120_678+121del
XM_006717002.4:c.843+120_843+121del (FANCC)	XP_006717065.1:n.843+120_843+121del
XM_006717004.4:c.843+120_843+121del (FANCC)	XP_006717067.1:n.843+120_843+121del
XM_011518365.3:c.843+120_843+121del (FANCC)	XP_011516667.1:n.843+120_843+121del
XM_011518366.3:c.843+120_843+121del (FANCC)	XP_011516668.1:n.843+120_843+121del
XM_011518367.2:c.387+120_387+121del (FANCC)	XP_011516669.1:n.387+120_387+121del
XM_011519121.3:c.2320-11980_2320-11979del (AOPEP)	XP_011517423.1:n.2320-11980_2320-11979del
XM_017014452.2:c.387+120_387+121del (FANCC)	XP_016869941.1:n.387+120_387+121del
XM_017014453.1:c.387+120_387+121del (FANCC)	XP_016869942.1:n.387+120_387+121del
XM_017014454.1:c.222+120_222+121del (FANCC)	XP_016869943.1:n.222+120_222+121del
XM_024447451.1:c.843+120_843+121del (FANCC)	XP_024303219.1:n.843+120_843+121del
NM_000136.3:c.843+120_843+121del (FANCC) MANE Select	NP_000127.2:n.843+120_843+121del
NM_001243743.2:c.843+120_843+121del (FANCC)	NP_001230672.1:n.843+120_843+121del
NM_001243744.2:c.843+120_843+121del (FANCC)	NP_001230673.1:n.843+120_843+121del