Canonical Allele Identifier: CA2133613497
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45154661_45154665delinsATTAT , CM000676.2:g.45154661_45154665delinsATTAT GRCh38
NC_000014.8:g.45623864_45623868delinsATTAT , CM000676.1:g.45623864_45623868delinsATTAT GRCh37
NC_000014.7:g.44693614_44693618delinsATTAT NCBI36
NG_007417.1:g.23729_23733delinsATTAT , LRG_502:g.23729_23733delinsATTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000556036.6:c.1184-36_1184-32delinsATTAT ENSP00000450596.1:n.1184-36_1184-32delins...
ENST00000556250.6:c.1184-36_1184-32delinsATTAT ENSP00000452033.2:n.1184-36_1184-32delins...
ENST00000696641.1:c.1025-36_1025-32delinsATTAT ENSP00000512774.1:n.1025-36_1025-32delins...
ENST00000696642.1:c.1051-36_1051-32delinsATTAT ENSP00000512775.1:n.1051-36_1051-32delins...
ENST00000696643.1:c.1184-36_1184-32delinsATTAT ENSP00000512776.1:n.1184-36_1184-32delins...
ENST00000696646.1:c.973-36_973-32delinsATTAT ENSP00000512777.1:n.973-36_973-32delinsAT...
ENST00000696647.1:c.1184-36_1184-32delinsATTAT ENSP00000512778.1:n.1184-36_1184-32delins...
ENST00000696648.1:c.1184-36_1184-32delinsATTAT ENSP00000512779.1:n.1184-36_1184-32delins...
ENST00000696649.1:c.1184-36_1184-32delinsATTAT ENSP00000512780.1:n.1184-36_1184-32delins...
ENST00000696650.1:n.1132-36_1132-32delinsATTAT
ENST00000696657.1:c.*402-36_*402-32delinsATTAT ENSP00000512784.1:n.*402-36_*402-32delins...
ENST00000696658.1:n.1734-36_1734-32delinsATTAT
ENST00000696662.1:c.1106-36_1106-32delinsATTAT ENSP00000512788.1:n.1106-36_1106-32delins...
ENST00000696675.1:c.1184-36_1184-32delinsATTAT ENSP00000512799.1:n.1184-36_1184-32delins...
ENST00000696680.1:c.1052-36_1052-32delinsATTAT ENSP00000512803.1:n.1052-36_1052-32delins...
ENST00000696681.1:c.1051-36_1051-32delinsATTAT ENSP00000512804.1:n.1051-36_1051-32delins...
ENST00000696682.1:c.1184-36_1184-32delinsATTAT ENSP00000512805.1:n.1184-36_1184-32delins...
ENST00000267430.10:c.1184-36_1184-32delinsATTAT MANE Select ENSP00000267430.5:n.1184-36_1184-32delins...
ENST00000267430.9:c.1184-36_1184-32delinsATTAT ENSP00000267430.5:n.1184-36_1184-32delins...
ENST00000542564.6:c.1106-36_1106-32delinsATTAT ENSP00000442493.2:n.1106-36_1106-32delins...
ENST00000556036.5:c.1184-36_1184-32delinsATTAT ENSP00000450596.1:n.1184-36_1184-32delins...
NM_001308133.1:c.1106-36_1106-32delinsATTAT NP_001295062.1:n.1106-36_1106-32delinsATT...
NM_001308134.1:c.1184-36_1184-32delinsATTAT NP_001295063.1:n.1184-36_1184-32delinsATT...
NM_020937.2:c.1184-36_1184-32delinsATTAT , LRG_502t1:c.1184-36_1184-32delinsATTAT NP_065988.1:n.1184-36_1184-32delinsATTAT
NM_020937.3:c.1184-36_1184-32delinsATTAT NP_065988.1:n.1184-36_1184-32delinsATTAT
XM_011537034.1:c.1184-36_1184-32delinsATTAT XP_011535336.1:n.1184-36_1184-32delinsATT...
XM_011537035.1:c.1106-36_1106-32delinsATTAT XP_011535337.1:n.1106-36_1106-32delinsATT...
XM_011537036.1:c.1184-36_1184-32delinsATTAT XP_011535338.1:n.1184-36_1184-32delinsATT...
XM_011537034.2:c.1184-36_1184-32delinsATTAT XP_011535336.1:n.1184-36_1184-32delinsATT...
XM_011537035.3:c.1106-36_1106-32delinsATTAT XP_011535337.1:n.1106-36_1106-32delinsATT...
XM_017021523.1:c.1184-36_1184-32delinsATTAT XP_016877012.1:n.1184-36_1184-32delinsATT...
XM_017021524.2:c.221-36_221-32delinsATTAT XP_016877013.1:n.221-36_221-32delinsATTAT...
XM_017021525.2:c.-2-36_-2-32delinsATTAT XP_016877014.1:n.-2-36_-2-32delinsATTAT
XM_017021526.2:c.-2-36_-2-32delinsATTAT XP_016877015.1:n.-2-36_-2-32delinsATTAT
XM_017021527.1:c.-2-36_-2-32delinsATTAT XP_016877016.1:n.-2-36_-2-32delinsATTAT
XR_001750470.1:n.1276-36_1276-32delinsATTAT
XR_001750471.2:n.1276-36_1276-32delinsATTAT
XR_001750472.1:n.1276-36_1276-32delinsATTAT
NM_020937.4:c.1184-36_1184-32delinsATTAT MANE Select NP_065988.1:n.1184-36_1184-32delinsATTAT
NM_001308133.2:c.1106-36_1106-32delinsATTAT NP_001295062.1:n.1106-36_1106-32delinsATT...
NM_001308134.2:c.1184-36_1184-32delinsATTAT NP_001295063.1:n.1184-36_1184-32delinsATT...