Canonical Allele Identifier: CA3771751

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35466243G>A , CM000668.2:g.35466243G>A	GRCh38
NC_000006.11:g.35434020G>A , CM000668.1:g.35434020G>A	GRCh37
NC_000006.10:g.35541998G>A	NCBI36
NG_011708.1:g.18883G>A , LRG_498:g.18883G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021922.3:c.1510-1G>A MANE Select	NP_068741.1:n.1510-1G>A
ENST00000229769.3:c.1510-1G>A MANE Select	ENSP00000229769.2:n.1510-1G>A
NM_021922.2:c.1510-1G>A , LRG_498t1:c.1510-1G>A	NP_068741.1:n.1510-1G>A
ENST00000229769.2:c.1510-1G>A	ENSP00000229769.2:n.1510-1G>A
ENST00000648059.1:c.*131-1G>A	ENSP00000497902.1:n.*131-1G>A
ENST00000696264.1:c.1317-1G>A	ENSP00000512511.1:n.1317-1G>A
ENST00000696265.1:c.1443-1G>A	ENSP00000512512.1:n.1443-1G>A
ENST00000696266.1:c.1155-1G>A	ENSP00000512513.1:n.1155-1G>A
ENST00000696267.1:n.1777-1G>A
ENST00000696269.1:n.1126-1G>A
XM_005248885.2:c.1489-1G>A	XP_005248942.1:n.1489-1G>A
XM_005248886.2:c.1441-1G>A	XP_005248943.1:n.1441-1G>A
XM_005248887.2:c.1384-1G>A	XP_005248944.1:n.1384-1G>A
XM_005248888.2:c.1317-1G>A	XP_005248945.1:n.1317-1G>A
XM_005248888.3:c.1317-1G>A	XP_005248945.1:n.1317-1G>A
XM_011514343.1:c.1216-1G>A	XP_011512645.1:n.1216-1G>A
XM_011514343.2:c.1216-1G>A	XP_011512645.1:n.1216-1G>A
XM_011514344.1:c.1216-1G>A	XP_011512646.1:n.1216-1G>A
XR_001743226.1:n.1650-1G>A
XR_002956267.1:n.1944-1G>A