Canonical Allele Identifier: CA1620905548

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456062_35456065delinsAGAG , CM000668.2:g.35456062_35456065delinsAGAG	GRCh38
NC_000006.11:g.35423839_35423842delinsAGAG , CM000668.1:g.35423839_35423842delinsAGAG	GRCh37
NC_000006.10:g.35531817_35531820delinsAGAG	NCBI36
NG_011708.1:g.8702_8705delinsAGAG , LRG_498:g.8702_8705delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.564_567delinsAGAG	ENSP00000512511.1:p.Glu188=
ENST00000696265.1:c.564_567delinsAGAG	ENSP00000512512.1:p.Glu188=
ENST00000696266.1:c.282_285delinsAGAG	ENSP00000512513.1:p.Glu94=
ENST00000696267.1:n.204_207delinsAGAG
ENST00000229769.3:c.564_567delinsAGAG MANE Select	ENSP00000229769.2:p.Glu188=
ENST00000648059.1:c.564_567delinsAGAG	ENSP00000497902.1:p.Glu188=
ENST00000229769.2:c.564_567delinsAGAG	ENSP00000229769.2:p.Glu188=
NM_021922.2:c.564_567delinsAGAG , LRG_498t1:c.564_567delinsAGAG	NP_068741.1:p.Glu188=
XM_005248885.2:c.564_567delinsAGAG	XP_005248942.1:p.Glu188=
XM_005248886.2:c.564_567delinsAGAG	XP_005248943.1:p.Glu188=
XM_005248887.2:c.564_567delinsAGAG	XP_005248944.1:p.Glu188=
XM_005248888.2:c.564_567delinsAGAG	XP_005248945.1:p.Glu188=
XM_011514343.1:c.270_273delinsAGAG	XP_011512645.1:p.Glu90=
XM_011514344.1:c.270_273delinsAGAG	XP_011512646.1:p.Glu90=
XM_005248888.3:c.564_567delinsAGAG	XP_005248945.1:p.Glu188=
XM_011514343.2:c.270_273delinsAGAG	XP_011512645.1:p.Glu90=
XR_001743226.1:n.771_774delinsAGAG
XR_002956267.1:n.771_774delinsAGAG
NM_021922.3:c.564_567delinsAGAG MANE Select	NP_068741.1:p.Glu188=