Canonical Allele Identifier: CA363773521

Gene: FANCE

Linked Data

• MyVariant Identifiers: chr6:g.35423942T>A (hg19) ; chr6:g.35456165T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456165T>A , CM000668.2:g.35456165T>A	GRCh38
NC_000006.11:g.35423942T>A , CM000668.1:g.35423942T>A	GRCh37
NC_000006.10:g.35531920T>A	NCBI36
NG_011708.1:g.8805T>A , LRG_498:g.8805T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.667T>A	ENSP00000512511.1:p.Trp223Arg
ENST00000696265.1:c.667T>A	ENSP00000512512.1:p.Trp223Arg
ENST00000696266.1:c.385T>A	ENSP00000512513.1:p.Trp129Arg
ENST00000696267.1:n.307T>A
ENST00000229769.3:c.667T>A MANE Select	ENSP00000229769.2:p.Trp223Arg
ENST00000648059.1:c.667T>A	ENSP00000497902.1:p.Trp223Arg
ENST00000229769.2:c.667T>A	ENSP00000229769.2:p.Trp223Arg
NM_021922.2:c.667T>A , LRG_498t1:c.667T>A	NP_068741.1:p.Trp223Arg
XM_005248885.2:c.667T>A	XP_005248942.1:p.Trp223Arg
XM_005248886.2:c.667T>A	XP_005248943.1:p.Trp223Arg
XM_005248887.2:c.667T>A	XP_005248944.1:p.Trp223Arg
XM_005248888.2:c.667T>A	XP_005248945.1:p.Trp223Arg
XM_011514343.1:c.373T>A	XP_011512645.1:p.Trp125Arg
XM_011514344.1:c.373T>A	XP_011512646.1:p.Trp125Arg
XM_005248888.3:c.667T>A	XP_005248945.1:p.Trp223Arg
XM_011514343.2:c.373T>A	XP_011512645.1:p.Trp125Arg
XR_001743226.1:n.874T>A
XR_002956267.1:n.874T>A
NM_021922.3:c.667T>A MANE Select	NP_068741.1:p.Trp223Arg