Canonical Allele Identifier: CA1865438082

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135357_95135358delinsCT , CM000671.2:g.95135357_95135358delinsCT	GRCh38
NC_000009.11:g.97897639_97897640delinsCT , CM000671.1:g.97897639_97897640delinsCT	GRCh37
NC_000009.10:g.96937460_96937461delinsCT	NCBI36
NG_011707.1:g.187352_187353delinsAG , LRG_497:g.187352_187353delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-11854_411-11853delinsCT (AOPEP)
ENST00000696261.1:n.1222_1223delinsAG (FANCC)
ENST00000289081.8:c.831_832delinsAG (FANCC) MANE Select	ENSP00000289081.3:p.Lys277=
ENST00000375305.6:c.831_832delinsAG (FANCC)	ENSP00000364454.1:p.Lys277=
ENST00000490972.7:c.831_832delinsAG (FANCC)	ENSP00000479931.1:p.Lys277=
ENST00000649334.1:c.976_977delinsAG (FANCC)	ENSP00000497735.1:n.976_977delinsAG
ENST00000649701.1:n.546_547delinsAG (FANCC)
ENST00000289081.7:c.831_832delinsAG (FANCC)	ENSP00000289081.3:p.Lys277=
ENST00000375305.5:c.831_832delinsAG (FANCC)	ENSP00000364454.1:p.Lys277=
ENST00000477942.5:n.186_187delinsAG (FANCC)
ENST00000480712.5:n.16_17delinsAG (FANCC)
ENST00000490972.6:c.831_832delinsAG (FANCC)	ENSP00000479931.1:p.Lys277=
NM_000136.2:c.831_832delinsAG , LRG_497t1:c.831_832delinsAG (FANCC)	NP_000127.2:p.Lys277=
NM_001243743.1:c.831_832delinsAG (FANCC)	NP_001230672.1:p.Lys277=
NM_001243744.1:c.831_832delinsAG (FANCC)	NP_001230673.1:p.Lys277=
XM_005251802.2:c.150_151delinsAG (FANCC)	XP_005251859.1:p.Lys50=
XM_006717001.1:c.666_667delinsAG (FANCC)	XP_006717064.1:p.Lys222=
XM_006717002.2:c.831_832delinsAG (FANCC)	XP_006717065.1:p.Lys277=
XM_006717004.2:c.831_832delinsAG (FANCC)	XP_006717067.1:p.Lys277=
XM_011518365.1:c.831_832delinsAG (FANCC)	XP_011516667.1:p.Lys277=
XM_011518366.1:c.831_832delinsAG (FANCC)	XP_011516668.1:p.Lys277=
XM_011518367.1:c.375_376delinsAG (FANCC)	XP_011516669.1:p.Lys125=
XM_011519121.1:c.2320-11854_2320-11853delinsCT (AOPEP)	XP_011517423.1:n.2320-11854_2320-11853delinsCT
XM_005251802.3:c.150_151delinsAG (FANCC)	XP_005251859.1:p.Lys50=
XM_006717001.3:c.666_667delinsAG (FANCC)	XP_006717064.1:p.Lys222=
XM_006717002.4:c.831_832delinsAG (FANCC)	XP_006717065.1:p.Lys277=
XM_006717004.4:c.831_832delinsAG (FANCC)	XP_006717067.1:p.Lys277=
XM_011518365.3:c.831_832delinsAG (FANCC)	XP_011516667.1:p.Lys277=
XM_011518366.3:c.831_832delinsAG (FANCC)	XP_011516668.1:p.Lys277=
XM_011518367.2:c.375_376delinsAG (FANCC)	XP_011516669.1:p.Lys125=
XM_011519121.3:c.2320-11854_2320-11853delinsCT (AOPEP)	XP_011517423.1:n.2320-11854_2320-11853delinsCT
XM_017014452.2:c.375_376delinsAG (FANCC)	XP_016869941.1:p.Lys125=
XM_017014453.1:c.375_376delinsAG (FANCC)	XP_016869942.1:p.Lys125=
XM_017014454.1:c.210_211delinsAG (FANCC)	XP_016869943.1:p.Lys70=
XM_024447451.1:c.831_832delinsAG (FANCC)	XP_024303219.1:p.Lys277=
NM_000136.3:c.831_832delinsAG (FANCC) MANE Select	NP_000127.2:p.Lys277=
NM_001243743.2:c.831_832delinsAG (FANCC)	NP_001230672.1:p.Lys277=
NM_001243744.2:c.831_832delinsAG (FANCC)	NP_001230673.1:p.Lys277=