Canonical Allele Identifier: CA449942262

Gene: FANCE

Linked Data

• MyVariant Identifiers: chr6:g.35423542A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455765A>C , CM000668.2:g.35455765A>C	GRCh38
NC_000006.11:g.35423542A>C , CM000668.1:g.35423542A>C	GRCh37
NC_000006.10:g.35531520A>C	NCBI36
NG_011708.1:g.8405A>C , LRG_498:g.8405A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.267A>C	ENSP00000512511.1:p.Arg89=
ENST00000696265.1:c.267A>C	ENSP00000512512.1:p.Arg89=
ENST00000229769.3:c.267A>C MANE Select	ENSP00000229769.2:p.Arg89=
ENST00000648059.1:c.267A>C	ENSP00000497902.1:p.Arg89=
ENST00000229769.2:c.267A>C	ENSP00000229769.2:p.Arg89=
NM_021922.2:c.267A>C , LRG_498t1:c.267A>C	NP_068741.1:p.Arg89=
XM_005248885.2:c.267A>C	XP_005248942.1:p.Arg89=
XM_005248886.2:c.267A>C	XP_005248943.1:p.Arg89=
XM_005248887.2:c.267A>C	XP_005248944.1:p.Arg89=
XM_005248888.2:c.267A>C	XP_005248945.1:p.Arg89=
XM_011514343.1:c.-28A>C	XP_011512645.1:n.-28A>C
XM_011514344.1:c.-28A>C	XP_011512646.1:n.-28A>C
XM_005248888.3:c.267A>C	XP_005248945.1:p.Arg89=
XM_011514343.2:c.-28A>C	XP_011512645.1:n.-28A>C
XR_001743226.1:n.474A>C
XR_002956267.1:n.474A>C
NM_021922.3:c.267A>C MANE Select	NP_068741.1:p.Arg89=