Canonical Allele Identifier: CA2695206215

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456149del , CM000668.2:g.35456149del	GRCh38
NC_000006.11:g.35423926del , CM000668.1:g.35423926del	GRCh37
NC_000006.10:g.35531904del	NCBI36
NG_011708.1:g.8789del , LRG_498:g.8789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.651del	ENSP00000512511.1:p.Arg219AspfsTer?
ENST00000696265.1:c.651del	ENSP00000512512.1:p.Arg219AspfsTer?
ENST00000696266.1:c.369del	ENSP00000512513.1:p.Arg125AspfsTer?
ENST00000696267.1:n.291del
ENST00000229769.3:c.651del MANE Select	ENSP00000229769.2:p.Arg219AspfsTer?
ENST00000648059.1:c.651del	ENSP00000497902.1:p.Arg219AspfsTer?
ENST00000229769.2:c.651del	ENSP00000229769.2:p.Arg219AspfsTer?
NM_021922.2:c.651del , LRG_498t1:c.651del	NP_068741.1:p.Arg219AspfsTer?
XM_005248885.2:c.651del	XP_005248942.1:p.Arg219AspfsTer?
XM_005248886.2:c.651del	XP_005248943.1:p.Arg219AspfsTer?
XM_005248887.2:c.651del	XP_005248944.1:p.Arg219AspfsTer?
XM_005248888.2:c.651del	XP_005248945.1:p.Arg219AspfsTer?
XM_011514343.1:c.357del	XP_011512645.1:p.Arg121AspfsTer?
XM_011514344.1:c.357del	XP_011512646.1:p.Arg121AspfsTer?
XM_005248888.3:c.651del	XP_005248945.1:p.Arg219AspfsTer?
XM_011514343.2:c.357del	XP_011512645.1:p.Arg121AspfsTer?
XR_001743226.1:n.858del
XR_002956267.1:n.858del
NM_021922.3:c.651del MANE Select	NP_068741.1:p.Arg219AspfsTer?