Canonical Allele Identifier: CA3771661

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35459753A>G , CM000668.2:g.35459753A>G	GRCh38
NC_000006.11:g.35427530A>G , CM000668.1:g.35427530A>G	GRCh37
NC_000006.10:g.35535508A>G	NCBI36
NG_011708.1:g.12393A>G , LRG_498:g.12393A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.1309A>G	ENSP00000512511.1:p.Met437Val
ENST00000696265.1:c.1309A>G	ENSP00000512512.1:p.Met437Val
ENST00000696266.1:c.958A>G	ENSP00000512513.1:p.Met320Val
ENST00000696267.1:n.1576A>G
ENST00000696268.1:n.169A>G
ENST00000229769.3:c.1309A>G MANE Select	ENSP00000229769.2:p.Met437Val
ENST00000648059.1:c.1309A>G	ENSP00000497902.1:p.Met437Val
ENST00000229769.2:c.1309A>G	ENSP00000229769.2:p.Met437Val
NM_021922.2:c.1309A>G , LRG_498t1:c.1309A>G	NP_068741.1:p.Met437Val
XM_005248885.2:c.1288A>G	XP_005248942.1:p.Met430Val
XM_005248886.2:c.1240A>G	XP_005248943.1:p.Met414Val
XM_005248887.2:c.1309A>G	XP_005248944.1:p.Met437Val
XM_005248888.2:c.1309A>G	XP_005248945.1:p.Met437Val
XM_011514343.1:c.1015A>G	XP_011512645.1:p.Met339Val
XM_011514344.1:c.1015A>G	XP_011512646.1:p.Met339Val
XM_005248888.3:c.1309A>G	XP_005248945.1:p.Met437Val
XM_011514343.2:c.1015A>G	XP_011512645.1:p.Met339Val
XR_001743226.1:n.1516A>G
XR_002956267.1:n.1810A>G
NM_021922.3:c.1309A>G MANE Select	NP_068741.1:p.Met437Val