Canonical Allele Identifier: CA2133624517
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185287A= , CM000676.2:g.45185287A= GRCh38
NC_000014.8:g.45654490A= , CM000676.1:g.45654490A= GRCh37
NC_000014.7:g.44724240A= NCBI36
NG_007417.1:g.54355A= , LRG_502:g.54355A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2798A= ENSP00000450632.2:p.Asp933=
ENST00000555484.2:c.364A=
ENST00000556250.6:c.4379A= ENSP00000452033.2:p.Asp1460=
ENST00000557110.2:c.364A=
ENST00000696642.1:c.*3397A= ENSP00000512775.1:n.*3397A=
ENST00000696644.1:n.322A=
ENST00000696645.1:n.476A=
ENST00000696647.1:c.4586A= ENSP00000512778.1:p.Asp1529=
ENST00000696648.1:c.*2611A= ENSP00000512779.1:n.*2611A=
ENST00000696649.1:c.4430A= ENSP00000512780.1:p.Asp1477=
ENST00000696650.1:n.4534A=
ENST00000696659.1:c.2584A=
ENST00000696663.1:c.3517A=
ENST00000696664.1:c.3418A=
ENST00000696665.1:c.364A=
ENST00000696675.1:c.*342A= ENSP00000512799.1:n.*342A=
ENST00000696683.1:c.3403A=
ENST00000696684.1:c.3403A=
ENST00000696685.1:c.3403A=
ENST00000696686.1:n.1323A=
ENST00000267430.10:c.4586A= MANE Select ENSP00000267430.5:p.Asp1529=
ENST00000267430.9:c.4586A= ENSP00000267430.5:p.Asp1529=
ENST00000542564.6:c.4508A= ENSP00000442493.2:p.Asp1503=
ENST00000554809.5:c.1383A=
ENST00000555013.1:n.419A=
ENST00000556250.5:c.3134A= ENSP00000452033.1:p.Asp1045=
NM_001308133.1:c.4508A= NP_001295062.1:p.Asp1503=
NM_020937.2:c.4586A= , LRG_502t1:c.4586A= NP_065988.1:p.Asp1529=
NM_020937.3:c.4586A= NP_065988.1:p.Asp1529=
XM_011537034.1:c.4601A= XP_011535336.1:p.Asp1534=
XM_011537035.1:c.4523A= XP_011535337.1:p.Asp1508=
XM_011537036.1:c.4601A= XP_011535338.1:p.Asp1534=
XM_011537037.1:c.2615A= XP_011535339.1:p.Asp872=
XM_011537034.2:c.4601A= XP_011535336.1:p.Asp1534=
XM_011537035.3:c.4523A= XP_011535337.1:p.Asp1508=
XM_011537037.3:c.2615A= XP_011535339.1:p.Asp872=
XM_017021523.1:c.4601A= XP_016877012.1:p.Asp1534=
XM_017021524.2:c.3638A= XP_016877013.1:p.Asp1213=
XM_017021525.2:c.3416A= XP_016877014.1:p.Asp1139=
XM_017021526.2:c.3416A= XP_016877015.1:p.Asp1139=
XM_017021527.1:c.3401A= XP_016877016.1:p.Asp1134=
XR_001750470.1:n.4693A=
XR_001750471.2:n.4678A=
XR_001750472.1:n.4730A=
NM_020937.4:c.4586A= MANE Select NP_065988.1:p.Asp1529=
NM_001308133.2:c.4508A= NP_001295062.1:p.Asp1503=