Canonical Allele Identifier: CA1865468816

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95149968A= , CM000671.2:g.95149968A=	GRCh38
NC_000009.11:g.97912250A= , CM000671.1:g.97912250A=	GRCh37
NC_000009.10:g.96952071A=	NCBI36
NG_011707.1:g.172742T= , LRG_497:g.172742T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.3168A= (AOPEP)
ENST00000696261.1:n.1032T= (FANCC)
ENST00000289081.8:c.641T= (FANCC) MANE Select	ENSP00000289081.3:p.Ile214=
ENST00000375305.6:c.641T= (FANCC)	ENSP00000364454.1:p.Ile214=
ENST00000490972.7:c.641T= (FANCC)	ENSP00000479931.1:p.Ile214=
ENST00000649334.1:c.786T= (FANCC)	ENSP00000497735.1:n.786T=
ENST00000649701.1:n.356T= (FANCC)
ENST00000289081.7:c.641T= (FANCC)	ENSP00000289081.3:p.Ile214=
ENST00000375305.5:c.641T= (FANCC)	ENSP00000364454.1:p.Ile214=
ENST00000490972.6:c.641T= (FANCC)	ENSP00000479931.1:p.Ile214=
ENST00000493098.1:n.66T= (FANCC)
NM_000136.2:c.641T= , LRG_497t1:c.641T= (FANCC)	NP_000127.2:p.Ile214=
NM_001243743.1:c.641T= (FANCC)	NP_001230672.1:p.Ile214=
NM_001243744.1:c.641T= (FANCC)	NP_001230673.1:p.Ile214=
XM_006717001.1:c.522-14466T= (FANCC)	XP_006717064.1:n.522-14466T=
XM_006717002.2:c.641T= (FANCC)	XP_006717065.1:p.Ile214=
XM_006717004.2:c.641T= (FANCC)	XP_006717067.1:p.Ile214=
XM_011518365.1:c.641T= (FANCC)	XP_011516667.1:p.Ile214=
XM_011518366.1:c.641T= (FANCC)	XP_011516668.1:p.Ile214=
XM_011518367.1:c.185T= (FANCC)	XP_011516669.1:p.Ile62=
XM_006717001.3:c.522-14466T= (FANCC)	XP_006717064.1:n.522-14466T=
XM_006717002.4:c.641T= (FANCC)	XP_006717065.1:p.Ile214=
XM_006717004.4:c.641T= (FANCC)	XP_006717067.1:p.Ile214=
XM_011518365.3:c.641T= (FANCC)	XP_011516667.1:p.Ile214=
XM_011518366.3:c.641T= (FANCC)	XP_011516668.1:p.Ile214=
XM_011518367.2:c.185T= (FANCC)	XP_011516669.1:p.Ile62=
XM_017014452.2:c.185T= (FANCC)	XP_016869941.1:p.Ile62=
XM_017014453.1:c.185T= (FANCC)	XP_016869942.1:p.Ile62=
XM_017014454.1:c.66-14466T= (FANCC)	XP_016869943.1:n.66-14466T=
XM_024447451.1:c.641T= (FANCC)	XP_024303219.1:p.Ile214=
NM_000136.3:c.641T= (FANCC) MANE Select	NP_000127.2:p.Ile214=
NM_001243743.2:c.641T= (FANCC)	NP_001230672.1:p.Ile214=
NM_001243744.2:c.641T= (FANCC)	NP_001230673.1:p.Ile214=