Canonical Allele Identifier: CA3771411

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455947T>C , CM000668.2:g.35455947T>C	GRCh38
NC_000006.11:g.35423724T>C , CM000668.1:g.35423724T>C	GRCh37
NC_000006.10:g.35531702T>C	NCBI36
NG_011708.1:g.8587T>C , LRG_498:g.8587T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021922.3:c.449T>C MANE Select	NP_068741.1:p.Met150Thr
ENST00000229769.3:c.449T>C MANE Select	ENSP00000229769.2:p.Met150Thr
NM_021922.2:c.449T>C , LRG_498t1:c.449T>C	NP_068741.1:p.Met150Thr
ENST00000229769.2:c.449T>C	ENSP00000229769.2:p.Met150Thr
ENST00000648059.1:c.449T>C	ENSP00000497902.1:p.Met150Thr
ENST00000696264.1:c.449T>C	ENSP00000512511.1:p.Met150Thr
ENST00000696265.1:c.449T>C	ENSP00000512512.1:p.Met150Thr
ENST00000696266.1:c.167T>C	ENSP00000512513.1:p.Met56Thr
ENST00000696267.1:n.89T>C
XM_005248885.2:c.449T>C	XP_005248942.1:p.Met150Thr
XM_005248886.2:c.449T>C	XP_005248943.1:p.Met150Thr
XM_005248887.2:c.449T>C	XP_005248944.1:p.Met150Thr
XM_005248888.2:c.449T>C	XP_005248945.1:p.Met150Thr
XM_005248888.3:c.449T>C	XP_005248945.1:p.Met150Thr
XM_011514343.1:c.155T>C	XP_011512645.1:p.Met52Thr
XM_011514343.2:c.155T>C	XP_011512645.1:p.Met52Thr
XM_011514344.1:c.155T>C	XP_011512646.1:p.Met52Thr
XR_001743226.1:n.656T>C
XR_002956267.1:n.656T>C