Canonical Allele Identifier: CA363777151

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35459722G>C , CM000668.2:g.35459722G>C	GRCh38
NC_000006.11:g.35427499G>C , CM000668.1:g.35427499G>C	GRCh37
NC_000006.10:g.35535477G>C	NCBI36
NG_011708.1:g.12362G>C , LRG_498:g.12362G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021922.3:c.1278G>C MANE Select	NP_068741.1:p.Met426Ile
ENST00000229769.3:c.1278G>C MANE Select	ENSP00000229769.2:p.Met426Ile
NM_021922.2:c.1278G>C , LRG_498t1:c.1278G>C	NP_068741.1:p.Met426Ile
ENST00000229769.2:c.1278G>C	ENSP00000229769.2:p.Met426Ile
ENST00000648059.1:c.1278G>C	ENSP00000497902.1:p.Met426Ile
ENST00000696264.1:c.1278G>C	ENSP00000512511.1:p.Met426Ile
ENST00000696265.1:c.1278G>C	ENSP00000512512.1:p.Met426Ile
ENST00000696266.1:c.927G>C	ENSP00000512513.1:p.Met309Ile
ENST00000696267.1:n.1545G>C
ENST00000696268.1:n.138G>C
XM_005248885.2:c.1257G>C	XP_005248942.1:p.Met419Ile
XM_005248886.2:c.1209G>C	XP_005248943.1:p.Met403Ile
XM_005248887.2:c.1278G>C	XP_005248944.1:p.Met426Ile
XM_005248888.2:c.1278G>C	XP_005248945.1:p.Met426Ile
XM_005248888.3:c.1278G>C	XP_005248945.1:p.Met426Ile
XM_011514343.1:c.984G>C	XP_011512645.1:p.Met328Ile
XM_011514343.2:c.984G>C	XP_011512645.1:p.Met328Ile
XM_011514344.1:c.984G>C	XP_011512646.1:p.Met328Ile
XR_001743226.1:n.1485G>C
XR_002956267.1:n.1779G>C