Canonical Allele Identifier: CA389591284

Gene: FANCM

Linked Data

• ClinVar Variation Id: 2431536
• ClinVar RCV Id: RCV003140590
• MyVariant Identifiers: chr14:g.45623977G>A (hg19) ; chr14:g.45154774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154774G>A , CM000676.2:g.45154774G>A	GRCh38
NC_000014.8:g.45623977G>A , CM000676.1:g.45623977G>A	GRCh37
NC_000014.7:g.44693727G>A	NCBI36
NG_007417.1:g.23842G>A , LRG_502:g.23842G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000556036.6:c.1261G>A	ENSP00000450596.1:p.Ala421Thr
ENST00000556250.6:c.1261G>A	ENSP00000452033.2:p.Ala421Thr
ENST00000696641.1:c.1102G>A	ENSP00000512774.1:p.Ala368Thr
ENST00000696642.1:c.*72G>A	ENSP00000512775.1:n.*72G>A
ENST00000696643.1:c.1261G>A	ENSP00000512776.1:p.Ala421Thr
ENST00000696646.1:c.*72G>A	ENSP00000512777.1:n.*72G>A
ENST00000696647.1:c.1261G>A	ENSP00000512778.1:p.Ala421Thr
ENST00000696648.1:c.1261G>A	ENSP00000512779.1:p.Ala421Thr
ENST00000696649.1:c.1261G>A	ENSP00000512780.1:p.Ala421Thr
ENST00000696650.1:n.1209G>A
ENST00000696657.1:c.*479G>A	ENSP00000512784.1:n.*479G>A
ENST00000696658.1:n.1811G>A
ENST00000696662.1:c.1183G>A	ENSP00000512788.1:p.Ala395Thr
ENST00000696663.1:c.78G>A
ENST00000696664.1:c.78G>A
ENST00000696675.1:c.1261G>A	ENSP00000512799.1:p.Ala421Thr
ENST00000696680.1:c.1129G>A	ENSP00000512803.1:p.Ala377Thr
ENST00000696681.1:c.*72G>A	ENSP00000512804.1:n.*72G>A
ENST00000696682.1:c.1261G>A	ENSP00000512805.1:p.Ala421Thr
ENST00000696683.1:c.78G>A
ENST00000696684.1:c.78G>A
ENST00000696685.1:c.78G>A
ENST00000267430.10:c.1261G>A MANE Select	ENSP00000267430.5:p.Ala421Thr
ENST00000267430.9:c.1261G>A	ENSP00000267430.5:p.Ala421Thr
ENST00000542564.6:c.1183G>A	ENSP00000442493.2:p.Ala395Thr
ENST00000556036.5:c.1261G>A	ENSP00000450596.1:p.Ala421Thr
ENST00000556250.5:c.16G>A	ENSP00000452033.1:p.Ala6Thr
NM_001308133.1:c.1183G>A	NP_001295062.1:p.Ala395Thr
NM_001308134.1:c.1261G>A	NP_001295063.1:p.Ala421Thr
NM_020937.2:c.1261G>A , LRG_502t1:c.1261G>A	NP_065988.1:p.Ala421Thr
NM_020937.3:c.1261G>A	NP_065988.1:p.Ala421Thr
XM_011537034.1:c.1261G>A	XP_011535336.1:p.Ala421Thr
XM_011537035.1:c.1183G>A	XP_011535337.1:p.Ala395Thr
XM_011537036.1:c.1261G>A	XP_011535338.1:p.Ala421Thr
XM_011537034.2:c.1261G>A	XP_011535336.1:p.Ala421Thr
XM_011537035.3:c.1183G>A	XP_011535337.1:p.Ala395Thr
XM_017021523.1:c.1261G>A	XP_016877012.1:p.Ala421Thr
XM_017021524.2:c.298G>A	XP_016877013.1:p.Ala100Thr
XM_017021525.2:c.76G>A	XP_016877014.1:p.Ala26Thr
XM_017021526.2:c.76G>A	XP_016877015.1:p.Ala26Thr
XM_017021527.1:c.76G>A	XP_016877016.1:p.Ala26Thr
XR_001750470.1:n.1353G>A
XR_001750471.2:n.1353G>A
XR_001750472.1:n.1353G>A
NM_020937.4:c.1261G>A MANE Select	NP_065988.1:p.Ala421Thr
NM_001308133.2:c.1183G>A	NP_001295062.1:p.Ala395Thr
NM_001308134.2:c.1261G>A	NP_001295063.1:p.Ala421Thr