Canonical Allele Identifier: CA2133614348
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45166869C= , CM000676.2:g.45166869C= GRCh38
NC_000014.8:g.45636072C= , CM000676.1:g.45636072C= GRCh37
NC_000014.7:g.44705822C= NCBI36
NG_007417.1:g.35937C= , LRG_502:g.35937C=

Transcript Alleles

HGVS Amino-acid change
ENST00000556036.6:c.1789-81C= ENSP00000450596.1:n.1789-81C=
ENST00000556250.6:c.1582-81C= ENSP00000452033.2:n.1582-81C=
ENST00000696641.1:c.1630-81C= ENSP00000512774.1:n.1630-81C=
ENST00000696642.1:c.*600-81C= ENSP00000512775.1:n.*600-81C=
ENST00000696646.1:c.*600-81C= ENSP00000512777.1:n.*600-81C=
ENST00000696647.1:c.1789-81C= ENSP00000512778.1:n.1789-81C=
ENST00000696648.1:c.1789-81C= ENSP00000512779.1:n.1789-81C=
ENST00000696649.1:c.1789-81C= ENSP00000512780.1:n.1789-81C=
ENST00000696650.1:n.1737-81C=
ENST00000696658.1:n.2339-81C=
ENST00000696662.1:c.1711-81C= ENSP00000512788.1:n.1711-81C=
ENST00000696663.1:c.606-81C=
ENST00000696664.1:c.606-81C=
ENST00000696675.1:c.1789-81C= ENSP00000512799.1:n.1789-81C=
ENST00000696683.1:c.606-81C=
ENST00000696684.1:c.606-81C=
ENST00000696685.1:c.606-81C=
ENST00000267430.10:c.1789-81C= MANE Select ENSP00000267430.5:n.1789-81C=
ENST00000267430.9:c.1789-81C= ENSP00000267430.5:n.1789-81C=
ENST00000542564.6:c.1711-81C= ENSP00000442493.2:n.1711-81C=
ENST00000556036.5:c.1789-81C= ENSP00000450596.1:n.1789-81C=
ENST00000556250.5:c.337-81C= ENSP00000452033.1:n.337-81C=
NM_001308133.1:c.1711-81C= NP_001295062.1:n.1711-81C=
NM_001308134.1:c.1789-81C= NP_001295063.1:n.1789-81C=
NM_020937.2:c.1789-81C= , LRG_502t1:c.1789-81C= NP_065988.1:n.1789-81C=
NM_020937.3:c.1789-81C= NP_065988.1:n.1789-81C=
XM_011537034.1:c.1789-81C= XP_011535336.1:n.1789-81C=
XM_011537035.1:c.1711-81C= XP_011535337.1:n.1711-81C=
XM_011537036.1:c.1789-81C= XP_011535338.1:n.1789-81C=
XM_011537034.2:c.1789-81C= XP_011535336.1:n.1789-81C=
XM_011537035.3:c.1711-81C= XP_011535337.1:n.1711-81C=
XM_017021523.1:c.1789-81C= XP_016877012.1:n.1789-81C=
XM_017021524.2:c.826-81C= XP_016877013.1:n.826-81C=
XM_017021525.2:c.604-81C= XP_016877014.1:n.604-81C=
XM_017021526.2:c.604-81C= XP_016877015.1:n.604-81C=
XM_017021527.1:c.604-81C= XP_016877016.1:n.604-81C=
XR_001750470.1:n.1881-81C=
XR_001750471.2:n.1881-81C=
XR_001750472.1:n.1881-81C=
NM_020937.4:c.1789-81C= MANE Select NP_065988.1:n.1789-81C=
NM_001308133.2:c.1711-81C= NP_001295062.1:n.1711-81C=
NM_001308134.2:c.1789-81C= NP_001295063.1:n.1789-81C=