Canonical Allele Identifier: CA1865462114

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107072G= , CM000671.2:g.95107072G=	GRCh38
NC_000009.11:g.97869354G= , CM000671.1:g.97869354G=	GRCh37
NC_000009.10:g.96909175G=	NCBI36
NG_011707.1:g.215638C= , LRG_497:g.215638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26292G= (AOPEP)
ENST00000696260.1:n.2342C= (FANCC)
ENST00000289081.8:c.1527C= (FANCC) MANE Select	ENSP00000289081.3:p.Ile509=
ENST00000375305.6:c.1527C= (FANCC)	ENSP00000364454.1:p.Ile509=
ENST00000649334.1:c.1672C= (FANCC)	ENSP00000497735.1:n.1672C=
ENST00000289081.7:c.1527C= (FANCC)	ENSP00000289081.3:p.Ile509=
ENST00000375305.5:c.1527C= (FANCC)	ENSP00000364454.1:p.Ile509=
NM_000136.2:c.1527C= , LRG_497t1:c.1527C= (FANCC)	NP_000127.2:p.Ile509=
NM_001243743.1:c.1527C= (FANCC)	NP_001230672.1:p.Ile509=
XM_005251802.2:c.846C= (FANCC)	XP_005251859.1:p.Ile282=
XM_006717001.1:c.1362C= (FANCC)	XP_006717064.1:p.Ile454=
XM_011518365.1:c.1527C= (FANCC)	XP_011516667.1:p.Ile509=
XM_011518367.1:c.1071C= (FANCC)	XP_011516669.1:p.Ile357=
XM_011519121.1:c.2319+26292G= (AOPEP)	XP_011517423.1:n.2319+26292G=
XM_005251802.3:c.846C= (FANCC)	XP_005251859.1:p.Ile282=
XM_006717001.3:c.1362C= (FANCC)	XP_006717064.1:p.Ile454=
XM_011518365.3:c.1527C= (FANCC)	XP_011516667.1:p.Ile509=
XM_011518367.2:c.1071C= (FANCC)	XP_011516669.1:p.Ile357=
XM_011519121.3:c.2319+26292G= (AOPEP)	XP_011517423.1:n.2319+26292G=
XM_017014452.2:c.1071C= (FANCC)	XP_016869941.1:p.Ile357=
XM_017014453.1:c.1071C= (FANCC)	XP_016869942.1:p.Ile357=
XM_017014454.1:c.906C= (FANCC)	XP_016869943.1:p.Ile302=
XM_024447451.1:c.1527C= (FANCC)	XP_024303219.1:p.Ile509=
XR_001746847.1:n.490G=
NM_000136.3:c.1527C= (FANCC) MANE Select	NP_000127.2:p.Ile509=
NM_001243743.2:c.1527C= (FANCC)	NP_001230672.1:p.Ile509=