Canonical Allele Identifier: CA2133607005

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159072_45159074delinsTAA , CM000676.2:g.45159072_45159074delinsTAA	GRCh38
NC_000014.8:g.45628275_45628277delinsTAA , CM000676.1:g.45628275_45628277delinsTAA	GRCh37
NC_000014.7:g.44698025_44698027delinsTAA	NCBI36
NG_007417.1:g.28140_28142delinsTAA , LRG_502:g.28140_28142delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1397-24_1397-22delinsTAA	ENSP00000450596.1:n.1397-24_1397-22delinsTAA
ENST00000556250.6:c.1397-24_1397-22delinsTAA	ENSP00000452033.2:n.1397-24_1397-22delinsTAA
ENST00000696641.1:c.1238-24_1238-22delinsTAA	ENSP00000512774.1:n.1238-24_1238-22delinsTAA
ENST00000696642.1:c.*208-24_*208-22delinsTAA	ENSP00000512775.1:n.*208-24_*208-22delinsTAA
ENST00000696643.1:c.1397-24_1397-22delinsTAA	ENSP00000512776.1:n.1397-24_1397-22delinsTAA
ENST00000696646.1:c.*208-24_*208-22delinsTAA	ENSP00000512777.1:n.*208-24_*208-22delinsTAA
ENST00000696647.1:c.1397-24_1397-22delinsTAA	ENSP00000512778.1:n.1397-24_1397-22delinsTAA
ENST00000696648.1:c.1397-24_1397-22delinsTAA	ENSP00000512779.1:n.1397-24_1397-22delinsTAA
ENST00000696649.1:c.1397-24_1397-22delinsTAA	ENSP00000512780.1:n.1397-24_1397-22delinsTAA
ENST00000696650.1:n.1345-24_1345-22delinsTAA
ENST00000696658.1:n.1947-24_1947-22delinsTAA
ENST00000696662.1:c.1319-24_1319-22delinsTAA	ENSP00000512788.1:n.1319-24_1319-22delinsTAA
ENST00000696663.1:c.214-24_214-22delinsTAA
ENST00000696664.1:c.214-24_214-22delinsTAA
ENST00000696675.1:c.1397-24_1397-22delinsTAA	ENSP00000512799.1:n.1397-24_1397-22delinsTAA
ENST00000696680.1:c.1265-24_1265-22delinsTAA	ENSP00000512803.1:n.1265-24_1265-22delinsTAA
ENST00000696681.1:c.*208-24_*208-22delinsTAA	ENSP00000512804.1:n.*208-24_*208-22delinsTAA
ENST00000696682.1:c.1397-24_1397-22delinsTAA	ENSP00000512805.1:n.1397-24_1397-22delinsTAA
ENST00000696683.1:c.214-24_214-22delinsTAA
ENST00000696684.1:c.214-24_214-22delinsTAA
ENST00000696685.1:c.214-24_214-22delinsTAA
ENST00000267430.10:c.1397-24_1397-22delinsTAA MANE Select	ENSP00000267430.5:n.1397-24_1397-22delinsTAA
ENST00000267430.9:c.1397-24_1397-22delinsTAA	ENSP00000267430.5:n.1397-24_1397-22delinsTAA
ENST00000542564.6:c.1319-24_1319-22delinsTAA	ENSP00000442493.2:n.1319-24_1319-22delinsTAA
ENST00000556036.5:c.1397-24_1397-22delinsTAA	ENSP00000450596.1:n.1397-24_1397-22delinsTAA
ENST00000556250.5:c.152-24_152-22delinsTAA	ENSP00000452033.1:n.152-24_152-22delinsTAA
NM_001308133.1:c.1319-24_1319-22delinsTAA	NP_001295062.1:n.1319-24_1319-22delinsTAA
NM_001308134.1:c.1397-24_1397-22delinsTAA	NP_001295063.1:n.1397-24_1397-22delinsTAA
NM_020937.2:c.1397-24_1397-22delinsTAA , LRG_502t1:c.1397-24_1397-22delinsTAA	NP_065988.1:n.1397-24_1397-22delinsTAA
NM_020937.3:c.1397-24_1397-22delinsTAA	NP_065988.1:n.1397-24_1397-22delinsTAA
XM_011537034.1:c.1397-24_1397-22delinsTAA	XP_011535336.1:n.1397-24_1397-22delinsTAA
XM_011537035.1:c.1319-24_1319-22delinsTAA	XP_011535337.1:n.1319-24_1319-22delinsTAA
XM_011537036.1:c.1397-24_1397-22delinsTAA	XP_011535338.1:n.1397-24_1397-22delinsTAA
XM_011537034.2:c.1397-24_1397-22delinsTAA	XP_011535336.1:n.1397-24_1397-22delinsTAA
XM_011537035.3:c.1319-24_1319-22delinsTAA	XP_011535337.1:n.1319-24_1319-22delinsTAA
XM_017021523.1:c.1397-24_1397-22delinsTAA	XP_016877012.1:n.1397-24_1397-22delinsTAA
XM_017021524.2:c.434-24_434-22delinsTAA	XP_016877013.1:n.434-24_434-22delinsTAA
XM_017021525.2:c.212-24_212-22delinsTAA	XP_016877014.1:n.212-24_212-22delinsTAA
XM_017021526.2:c.212-24_212-22delinsTAA	XP_016877015.1:n.212-24_212-22delinsTAA
XM_017021527.1:c.212-24_212-22delinsTAA	XP_016877016.1:n.212-24_212-22delinsTAA
XR_001750470.1:n.1489-24_1489-22delinsTAA
XR_001750471.2:n.1489-24_1489-22delinsTAA
XR_001750472.1:n.1489-24_1489-22delinsTAA
NM_020937.4:c.1397-24_1397-22delinsTAA MANE Select	NP_065988.1:n.1397-24_1397-22delinsTAA
NM_001308133.2:c.1319-24_1319-22delinsTAA	NP_001295062.1:n.1319-24_1319-22delinsTAA
NM_001308134.2:c.1397-24_1397-22delinsTAA	NP_001295063.1:n.1397-24_1397-22delinsTAA