Canonical Allele Identifier: CA363770497

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35452709G>A , CM000668.2:g.35452709G>A	GRCh38
NC_000006.11:g.35420486G>A , CM000668.1:g.35420486G>A	GRCh37
NC_000006.10:g.35528464G>A	NCBI36
NG_011708.1:g.5349G>A , LRG_498:g.5349G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021922.3:c.164G>A MANE Select	NP_068741.1:p.Trp55Ter
ENST00000229769.3:c.164G>A MANE Select	ENSP00000229769.2:p.Trp55Ter
NM_021922.2:c.164G>A , LRG_498t1:c.164G>A	NP_068741.1:p.Trp55Ter
ENST00000229769.2:c.164G>A	ENSP00000229769.2:p.Trp55Ter
ENST00000648059.1:c.164G>A	ENSP00000497902.1:p.Trp55Ter
ENST00000696264.1:c.164G>A	ENSP00000512511.1:p.Trp55Ter
ENST00000696265.1:c.164G>A	ENSP00000512512.1:p.Trp55Ter
XM_005248885.2:c.164G>A	XP_005248942.1:p.Trp55Ter
XM_005248886.2:c.164G>A	XP_005248943.1:p.Trp55Ter
XM_005248887.2:c.164G>A	XP_005248944.1:p.Trp55Ter
XM_005248888.2:c.164G>A	XP_005248945.1:p.Trp55Ter
XM_005248888.3:c.164G>A	XP_005248945.1:p.Trp55Ter
XR_001743226.1:n.371G>A
XR_002956267.1:n.371G>A