Canonical Allele Identifier: CA2624699561

Gene: FANCM

Linked Data

• gnomAD v4: 14-45185277-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185280del , CM000676.2:g.45185280del	GRCh38
NC_000014.8:g.45654483del , CM000676.1:g.45654483del	GRCh37
NC_000014.7:g.44724233del	NCBI36
NG_007417.1:g.54348del , LRG_502:g.54348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2791del	ENSP00000450632.2:p.Ser931HisfsTer20
ENST00000555484.2:c.357del
ENST00000556250.6:c.4372del	ENSP00000452033.2:p.Ser1458HisfsTer20
ENST00000557110.2:c.357del
ENST00000696642.1:c.*3390del	ENSP00000512775.1:n.*3390del
ENST00000696644.1:n.315del
ENST00000696645.1:n.469del
ENST00000696647.1:c.4579del	ENSP00000512778.1:p.Ser1527HisfsTer20
ENST00000696648.1:c.*2604del	ENSP00000512779.1:n.*2604del
ENST00000696649.1:c.4423del	ENSP00000512780.1:p.Ser1475HisfsTer20
ENST00000696650.1:n.4527del
ENST00000696659.1:c.2577del
ENST00000696663.1:c.3510del
ENST00000696664.1:c.3411del
ENST00000696665.1:c.357del
ENST00000696675.1:c.*335del	ENSP00000512799.1:n.*335del
ENST00000696683.1:c.3396del
ENST00000696684.1:c.3396del
ENST00000696685.1:c.3396del
ENST00000696686.1:n.1316del
ENST00000267430.10:c.4579del MANE Select	ENSP00000267430.5:p.Ser1527HisfsTer20
ENST00000267430.9:c.4579del	ENSP00000267430.5:p.Ser1527HisfsTer20
ENST00000542564.6:c.4501del	ENSP00000442493.2:p.Ser1501HisfsTer20
ENST00000554809.5:c.1376del
ENST00000555013.1:n.412del
ENST00000556250.5:c.3127del	ENSP00000452033.1:p.Ser1043HisfsTer20
NM_001308133.1:c.4501del	NP_001295062.1:p.Ser1501HisfsTer20
NM_020937.2:c.4579del , LRG_502t1:c.4579del	NP_065988.1:p.Ser1527HisfsTer20
NM_020937.3:c.4579del	NP_065988.1:p.Ser1527HisfsTer20
XM_011537034.1:c.4594del	XP_011535336.1:p.Ser1532HisfsTer20
XM_011537035.1:c.4516del	XP_011535337.1:p.Ser1506HisfsTer20
XM_011537036.1:c.4594del	XP_011535338.1:p.Ser1532HisfsTer20
XM_011537037.1:c.2608del	XP_011535339.1:p.Ser870HisfsTer20
XM_011537034.2:c.4594del	XP_011535336.1:p.Ser1532HisfsTer20
XM_011537035.3:c.4516del	XP_011535337.1:p.Ser1506HisfsTer20
XM_011537037.3:c.2608del	XP_011535339.1:p.Ser870HisfsTer20
XM_017021523.1:c.4594del	XP_016877012.1:p.Ser1532HisfsTer20
XM_017021524.2:c.3631del	XP_016877013.1:p.Ser1211HisfsTer20
XM_017021525.2:c.3409del	XP_016877014.1:p.Ser1137HisfsTer20
XM_017021526.2:c.3409del	XP_016877015.1:p.Ser1137HisfsTer20
XM_017021527.1:c.3394del	XP_016877016.1:p.Ser1132HisfsTer20
XR_001750470.1:n.4686del
XR_001750471.2:n.4671del
XR_001750472.1:n.4723del
NM_020937.4:c.4579del MANE Select	NP_065988.1:p.Ser1527HisfsTer20
NM_001308133.2:c.4501del	NP_001295062.1:p.Ser1501HisfsTer20