Canonical Allele Identifier: CA2624697645

Gene: FANCM

Linked Data

• gnomAD v4: 14-45154774-GCACGTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154781_45154786del , CM000676.2:g.45154781_45154786del	GRCh38
NC_000014.8:g.45623984_45623989del , CM000676.1:g.45623984_45623989del	GRCh37
NC_000014.7:g.44693734_44693739del	NCBI36
NG_007417.1:g.23849_23854del , LRG_502:g.23849_23854del

Transcript Alleles

HGVS	Amino-acid change
ENST00000556036.6:c.1268_1273del	ENSP00000450596.1:p.Thr423_Arg424del
ENST00000556250.6:c.1268_1273del	ENSP00000452033.2:p.Thr423_Arg424del
ENST00000696641.1:c.1109_1114del	ENSP00000512774.1:p.Thr370_Arg371del
ENST00000696642.1:c.*79_*84del	ENSP00000512775.1:n.*79_*84del
ENST00000696643.1:c.1268_1273del	ENSP00000512776.1:p.Thr423_Arg424del
ENST00000696646.1:c.*79_*84del	ENSP00000512777.1:n.*79_*84del
ENST00000696647.1:c.1268_1273del	ENSP00000512778.1:p.Thr423_Arg424del
ENST00000696648.1:c.1268_1273del	ENSP00000512779.1:p.Thr423_Arg424del
ENST00000696649.1:c.1268_1273del	ENSP00000512780.1:p.Thr423_Arg424del
ENST00000696650.1:n.1216_1221del
ENST00000696657.1:c.*486_*491del	ENSP00000512784.1:n.*486_*491del
ENST00000696658.1:n.1818_1823del
ENST00000696662.1:c.1190_1195del	ENSP00000512788.1:p.Thr397_Arg398del
ENST00000696663.1:c.85_90del
ENST00000696664.1:c.85_90del
ENST00000696675.1:c.1268_1273del	ENSP00000512799.1:p.Thr423_Arg424del
ENST00000696680.1:c.1136_1141del	ENSP00000512803.1:p.Thr379_Arg380del
ENST00000696681.1:c.*79_*84del	ENSP00000512804.1:n.*79_*84del
ENST00000696682.1:c.1268_1273del	ENSP00000512805.1:p.Thr423_Arg424del
ENST00000696683.1:c.85_90del
ENST00000696684.1:c.85_90del
ENST00000696685.1:c.85_90del
ENST00000267430.10:c.1268_1273del MANE Select	ENSP00000267430.5:p.Thr423_Arg424del
ENST00000267430.9:c.1268_1273del	ENSP00000267430.5:p.Thr423_Arg424del
ENST00000542564.6:c.1190_1195del	ENSP00000442493.2:p.Thr397_Arg398del
ENST00000556036.5:c.1268_1273del	ENSP00000450596.1:p.Thr423_Arg424del
ENST00000556250.5:c.23_28del	ENSP00000452033.1:p.Thr8_Arg9del
NM_001308133.1:c.1190_1195del	NP_001295062.1:p.Thr397_Arg398del
NM_001308134.1:c.1268_1273del	NP_001295063.1:p.Thr423_Arg424del
NM_020937.2:c.1268_1273del , LRG_502t1:c.1268_1273del	NP_065988.1:p.Thr423_Arg424del
NM_020937.3:c.1268_1273del	NP_065988.1:p.Thr423_Arg424del
XM_011537034.1:c.1268_1273del	XP_011535336.1:p.Thr423_Arg424del
XM_011537035.1:c.1190_1195del	XP_011535337.1:p.Thr397_Arg398del
XM_011537036.1:c.1268_1273del	XP_011535338.1:p.Thr423_Arg424del
XM_011537034.2:c.1268_1273del	XP_011535336.1:p.Thr423_Arg424del
XM_011537035.3:c.1190_1195del	XP_011535337.1:p.Thr397_Arg398del
XM_017021523.1:c.1268_1273del	XP_016877012.1:p.Thr423_Arg424del
XM_017021524.2:c.305_310del	XP_016877013.1:p.Thr102_Arg103del
XM_017021525.2:c.83_88del	XP_016877014.1:p.Thr28_Arg29del
XM_017021526.2:c.83_88del	XP_016877015.1:p.Thr28_Arg29del
XM_017021527.1:c.83_88del	XP_016877016.1:p.Thr28_Arg29del
XR_001750470.1:n.1360_1365del
XR_001750471.2:n.1360_1365del
XR_001750472.1:n.1360_1365del
NM_020937.4:c.1268_1273del MANE Select	NP_065988.1:p.Thr423_Arg424del
NM_001308133.2:c.1190_1195del	NP_001295062.1:p.Thr397_Arg398del
NM_001308134.2:c.1268_1273del	NP_001295063.1:p.Thr423_Arg424del