Canonical Allele Identifier: CA1865462204

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107247C= , CM000671.2:g.95107247C=	GRCh38
NC_000009.11:g.97869529C= , CM000671.1:g.97869529C=	GRCh37
NC_000009.10:g.96909350C=	NCBI36
NG_011707.1:g.215463G= , LRG_497:g.215463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26467C= (AOPEP)
ENST00000696260.1:n.2167G= (FANCC)
ENST00000289081.8:c.1352G= (FANCC) MANE Select	ENSP00000289081.3:p.Gly451=
ENST00000375305.6:c.1352G= (FANCC)	ENSP00000364454.1:p.Gly451=
ENST00000649334.1:c.1497G= (FANCC)	ENSP00000497735.1:n.1497G=
ENST00000289081.7:c.1352G= (FANCC)	ENSP00000289081.3:p.Gly451=
ENST00000375305.5:c.1352G= (FANCC)	ENSP00000364454.1:p.Gly451=
ENST00000464627.5:n.679G= (FANCC)
NM_000136.2:c.1352G= , LRG_497t1:c.1352G= (FANCC)	NP_000127.2:p.Gly451=
NM_001243743.1:c.1352G= (FANCC)	NP_001230672.1:p.Gly451=
XM_005251802.2:c.671G= (FANCC)	XP_005251859.1:p.Gly224=
XM_006717001.1:c.1187G= (FANCC)	XP_006717064.1:p.Gly396=
XM_011518365.1:c.1352G= (FANCC)	XP_011516667.1:p.Gly451=
XM_011518367.1:c.896G= (FANCC)	XP_011516669.1:p.Gly299=
XM_011519121.1:c.2319+26467C= (AOPEP)	XP_011517423.1:n.2319+26467C=
XM_005251802.3:c.671G= (FANCC)	XP_005251859.1:p.Gly224=
XM_006717001.3:c.1187G= (FANCC)	XP_006717064.1:p.Gly396=
XM_011518365.3:c.1352G= (FANCC)	XP_011516667.1:p.Gly451=
XM_011518367.2:c.896G= (FANCC)	XP_011516669.1:p.Gly299=
XM_011519121.3:c.2319+26467C= (AOPEP)	XP_011517423.1:n.2319+26467C=
XM_017014452.2:c.896G= (FANCC)	XP_016869941.1:p.Gly299=
XM_017014453.1:c.896G= (FANCC)	XP_016869942.1:p.Gly299=
XM_017014454.1:c.731G= (FANCC)	XP_016869943.1:p.Gly244=
XM_024447451.1:c.1352G= (FANCC)	XP_024303219.1:p.Gly451=
XR_001746847.1:n.665C=
NM_000136.3:c.1352G= (FANCC) MANE Select	NP_000127.2:p.Gly451=
NM_001243743.2:c.1352G= (FANCC)	NP_001230672.1:p.Gly451=