Canonical Allele Identifier: CA1620905434

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455829_35455830delinsGA , CM000668.2:g.35455829_35455830delinsGA	GRCh38
NC_000006.11:g.35423606_35423607delinsGA , CM000668.1:g.35423606_35423607delinsGA	GRCh37
NC_000006.10:g.35531584_35531585delinsGA	NCBI36
NG_011708.1:g.8469_8470delinsGA , LRG_498:g.8469_8470delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.331_332delinsGA	ENSP00000512511.1:p.Glu111=
ENST00000696265.1:c.331_332delinsGA	ENSP00000512512.1:p.Glu111=
ENST00000696266.1:c.49_50delinsGA	ENSP00000512513.1:p.Glu17=
ENST00000229769.3:c.331_332delinsGA MANE Select	ENSP00000229769.2:p.Glu111=
ENST00000648059.1:c.331_332delinsGA	ENSP00000497902.1:p.Glu111=
ENST00000229769.2:c.331_332delinsGA	ENSP00000229769.2:p.Glu111=
NM_021922.2:c.331_332delinsGA , LRG_498t1:c.331_332delinsGA	NP_068741.1:p.Glu111=
XM_005248885.2:c.331_332delinsGA	XP_005248942.1:p.Glu111=
XM_005248886.2:c.331_332delinsGA	XP_005248943.1:p.Glu111=
XM_005248887.2:c.331_332delinsGA	XP_005248944.1:p.Glu111=
XM_005248888.2:c.331_332delinsGA	XP_005248945.1:p.Glu111=
XM_011514343.1:c.37_38delinsGA	XP_011512645.1:p.Glu13=
XM_011514344.1:c.37_38delinsGA	XP_011512646.1:p.Glu13=
XM_005248888.3:c.331_332delinsGA	XP_005248945.1:p.Glu111=
XM_011514343.2:c.37_38delinsGA	XP_011512645.1:p.Glu13=
XR_001743226.1:n.538_539delinsGA
XR_002956267.1:n.538_539delinsGA
NM_021922.3:c.331_332delinsGA MANE Select	NP_068741.1:p.Glu111=