Canonical Allele Identifier: CA1620905511

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456004G= , CM000668.2:g.35456004G=	GRCh38
NC_000006.11:g.35423781G= , CM000668.1:g.35423781G=	GRCh37
NC_000006.10:g.35531759G=	NCBI36
NG_011708.1:g.8644G= , LRG_498:g.8644G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.506G=	ENSP00000512511.1:p.Arg169=
ENST00000696265.1:c.506G=	ENSP00000512512.1:p.Arg169=
ENST00000696266.1:c.224G=	ENSP00000512513.1:p.Arg75=
ENST00000696267.1:n.146G=
ENST00000229769.3:c.506G= MANE Select	ENSP00000229769.2:p.Arg169=
ENST00000648059.1:c.506G=	ENSP00000497902.1:p.Arg169=
ENST00000229769.2:c.506G=	ENSP00000229769.2:p.Arg169=
NM_021922.2:c.506G= , LRG_498t1:c.506G=	NP_068741.1:p.Arg169=
XM_005248885.2:c.506G=	XP_005248942.1:p.Arg169=
XM_005248886.2:c.506G=	XP_005248943.1:p.Arg169=
XM_005248887.2:c.506G=	XP_005248944.1:p.Arg169=
XM_005248888.2:c.506G=	XP_005248945.1:p.Arg169=
XM_011514343.1:c.212G=	XP_011512645.1:p.Arg71=
XM_011514344.1:c.212G=	XP_011512646.1:p.Arg71=
XM_005248888.3:c.506G=	XP_005248945.1:p.Arg169=
XM_011514343.2:c.212G=	XP_011512645.1:p.Arg71=
XR_001743226.1:n.713G=
XR_002956267.1:n.713G=
NM_021922.3:c.506G= MANE Select	NP_068741.1:p.Arg169=