Canonical Allele Identifier: CA1620905501

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455979_35455981delinsCAG , CM000668.2:g.35455979_35455981delinsCAG	GRCh38
NC_000006.11:g.35423756_35423758delinsCAG , CM000668.1:g.35423756_35423758delinsCAG	GRCh37
NC_000006.10:g.35531734_35531736delinsCAG	NCBI36
NG_011708.1:g.8619_8621delinsCAG , LRG_498:g.8619_8621delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.481_483delinsCAG	ENSP00000512511.1:p.Gln161=
ENST00000696265.1:c.481_483delinsCAG	ENSP00000512512.1:p.Gln161=
ENST00000696266.1:c.199_201delinsCAG	ENSP00000512513.1:p.Gln67=
ENST00000696267.1:n.121_123delinsCAG
ENST00000229769.3:c.481_483delinsCAG MANE Select	ENSP00000229769.2:p.Gln161=
ENST00000648059.1:c.481_483delinsCAG	ENSP00000497902.1:p.Gln161=
ENST00000229769.2:c.481_483delinsCAG	ENSP00000229769.2:p.Gln161=
NM_021922.2:c.481_483delinsCAG , LRG_498t1:c.481_483delinsCAG	NP_068741.1:p.Gln161=
XM_005248885.2:c.481_483delinsCAG	XP_005248942.1:p.Gln161=
XM_005248886.2:c.481_483delinsCAG	XP_005248943.1:p.Gln161=
XM_005248887.2:c.481_483delinsCAG	XP_005248944.1:p.Gln161=
XM_005248888.2:c.481_483delinsCAG	XP_005248945.1:p.Gln161=
XM_011514343.1:c.187_189delinsCAG	XP_011512645.1:p.Gln63=
XM_011514344.1:c.187_189delinsCAG	XP_011512646.1:p.Gln63=
XM_005248888.3:c.481_483delinsCAG	XP_005248945.1:p.Gln161=
XM_011514343.2:c.187_189delinsCAG	XP_011512645.1:p.Gln63=
XR_001743226.1:n.688_690delinsCAG
XR_002956267.1:n.688_690delinsCAG
NM_021922.3:c.481_483delinsCAG MANE Select	NP_068741.1:p.Gln161=