Canonical Allele Identifier: CA1620905587

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456161G= , CM000668.2:g.35456161G=	GRCh38
NC_000006.11:g.35423938G= , CM000668.1:g.35423938G=	GRCh37
NC_000006.10:g.35531916G=	NCBI36
NG_011708.1:g.8801G= , LRG_498:g.8801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.663G=	ENSP00000512511.1:p.Arg221=
ENST00000696265.1:c.663G=	ENSP00000512512.1:p.Arg221=
ENST00000696266.1:c.381G=	ENSP00000512513.1:p.Arg127=
ENST00000696267.1:n.303G=
ENST00000229769.3:c.663G= MANE Select	ENSP00000229769.2:p.Arg221=
ENST00000648059.1:c.663G=	ENSP00000497902.1:p.Arg221=
ENST00000229769.2:c.663G=	ENSP00000229769.2:p.Arg221=
NM_021922.2:c.663G= , LRG_498t1:c.663G=	NP_068741.1:p.Arg221=
XM_005248885.2:c.663G=	XP_005248942.1:p.Arg221=
XM_005248886.2:c.663G=	XP_005248943.1:p.Arg221=
XM_005248887.2:c.663G=	XP_005248944.1:p.Arg221=
XM_005248888.2:c.663G=	XP_005248945.1:p.Arg221=
XM_011514343.1:c.369G=	XP_011512645.1:p.Arg123=
XM_011514344.1:c.369G=	XP_011512646.1:p.Arg123=
XM_005248888.3:c.663G=	XP_005248945.1:p.Arg221=
XM_011514343.2:c.369G=	XP_011512645.1:p.Arg123=
XR_001743226.1:n.870G=
XR_002956267.1:n.870G=
NM_021922.3:c.663G= MANE Select	NP_068741.1:p.Arg221=