Canonical Allele Identifier: CA2133624399
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185170T= , CM000676.2:g.45185170T= GRCh38
NC_000014.8:g.45654373T= , CM000676.1:g.45654373T= GRCh37
NC_000014.7:g.44724123T= NCBI36
NG_007417.1:g.54238T= , LRG_502:g.54238T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2728-47T= ENSP00000450632.2:n.2728-47T=
ENST00000555484.2:c.294-47T=
ENST00000556250.6:c.4309-47T= ENSP00000452033.2:n.4309-47T=
ENST00000557110.2:c.294-47T=
ENST00000696642.1:c.*3327-47T= ENSP00000512775.1:n.*3327-47T=
ENST00000696644.1:n.252-47T=
ENST00000696645.1:n.406-47T=
ENST00000696647.1:c.4516-47T= ENSP00000512778.1:n.4516-47T=
ENST00000696648.1:c.*2541-47T= ENSP00000512779.1:n.*2541-47T=
ENST00000696649.1:c.4360-47T= ENSP00000512780.1:n.4360-47T=
ENST00000696650.1:n.4464-47T=
ENST00000696659.1:c.2514-47T=
ENST00000696663.1:c.3447-47T=
ENST00000696664.1:c.3348-47T=
ENST00000696665.1:c.294-47T=
ENST00000696675.1:c.*272-47T= ENSP00000512799.1:n.*272-47T=
ENST00000696683.1:c.3333-47T=
ENST00000696684.1:c.3333-47T=
ENST00000696685.1:c.3333-47T=
ENST00000696686.1:n.1253-47T=
ENST00000267430.10:c.4516-47T= MANE Select ENSP00000267430.5:n.4516-47T=
ENST00000267430.9:c.4516-47T= ENSP00000267430.5:n.4516-47T=
ENST00000542564.6:c.4438-47T= ENSP00000442493.2:n.4438-47T=
ENST00000554809.5:c.1313-47T=
ENST00000555013.1:n.349-47T=
ENST00000556250.5:c.3064-47T= ENSP00000452033.1:n.3064-47T=
NM_001308133.1:c.4438-47T= NP_001295062.1:n.4438-47T=
NM_020937.2:c.4516-47T= , LRG_502t1:c.4516-47T= NP_065988.1:n.4516-47T=
NM_020937.3:c.4516-47T= NP_065988.1:n.4516-47T=
XM_011537034.1:c.4531-47T= XP_011535336.1:n.4531-47T=
XM_011537035.1:c.4453-47T= XP_011535337.1:n.4453-47T=
XM_011537036.1:c.4531-47T= XP_011535338.1:n.4531-47T=
XM_011537037.1:c.2545-47T= XP_011535339.1:n.2545-47T=
XM_011537034.2:c.4531-47T= XP_011535336.1:n.4531-47T=
XM_011537035.3:c.4453-47T= XP_011535337.1:n.4453-47T=
XM_011537037.3:c.2545-47T= XP_011535339.1:n.2545-47T=
XM_017021523.1:c.4531-47T= XP_016877012.1:n.4531-47T=
XM_017021524.2:c.3568-47T= XP_016877013.1:n.3568-47T=
XM_017021525.2:c.3346-47T= XP_016877014.1:n.3346-47T=
XM_017021526.2:c.3346-47T= XP_016877015.1:n.3346-47T=
XM_017021527.1:c.3331-47T= XP_016877016.1:n.3331-47T=
XR_001750470.1:n.4623-47T=
XR_001750471.2:n.4608-47T=
XR_001750472.1:n.4660-47T=
NM_020937.4:c.4516-47T= MANE Select NP_065988.1:n.4516-47T=
NM_001308133.2:c.4438-47T= NP_001295062.1:n.4438-47T=