Canonical Allele Identifier: CA3771368

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455763C>T , CM000668.2:g.35455763C>T	GRCh38
NC_000006.11:g.35423540C>T , CM000668.1:g.35423540C>T	GRCh37
NC_000006.10:g.35531518C>T	NCBI36
NG_011708.1:g.8403C>T , LRG_498:g.8403C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021922.3:c.265C>T MANE Select	NP_068741.1:p.Arg89Ter
ENST00000229769.3:c.265C>T MANE Select	ENSP00000229769.2:p.Arg89Ter
NM_021922.2:c.265C>T , LRG_498t1:c.265C>T	NP_068741.1:p.Arg89Ter
ENST00000229769.2:c.265C>T	ENSP00000229769.2:p.Arg89Ter
ENST00000648059.1:c.265C>T	ENSP00000497902.1:p.Arg89Ter
ENST00000696264.1:c.265C>T	ENSP00000512511.1:p.Arg89Ter
ENST00000696265.1:c.265C>T	ENSP00000512512.1:p.Arg89Ter
XM_005248885.2:c.265C>T	XP_005248942.1:p.Arg89Ter
XM_005248886.2:c.265C>T	XP_005248943.1:p.Arg89Ter
XM_005248887.2:c.265C>T	XP_005248944.1:p.Arg89Ter
XM_005248888.2:c.265C>T	XP_005248945.1:p.Arg89Ter
XM_005248888.3:c.265C>T	XP_005248945.1:p.Arg89Ter
XM_011514343.1:c.-30C>T	XP_011512645.1:n.-30C>T
XM_011514343.2:c.-30C>T	XP_011512645.1:n.-30C>T
XM_011514344.1:c.-30C>T	XP_011512646.1:n.-30C>T
XR_001743226.1:n.472C>T
XR_002956267.1:n.472C>T