Canonical Allele Identifier: CA7169373

Gene: FANCM

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45175340_45175343del , CM000676.2:g.45175340_45175343del	GRCh38
NC_000014.8:g.45644543_45644546del , CM000676.1:g.45644543_45644546del	GRCh37
NC_000014.7:g.44714293_44714296del	NCBI36
NG_007417.1:g.44408_44411del , LRG_502:g.44408_44411del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.798_801del	ENSP00000450632.2:p.Lys267IlefsTer12
ENST00000556250.6:c.2379_2382del	ENSP00000452033.2:p.Lys794IlefsTer12
ENST00000696641.1:c.2427_2430del	ENSP00000512774.1:p.Lys810IlefsTer12
ENST00000696642.1:c.*1397_*1400del	ENSP00000512775.1:n.*1397_*1400del
ENST00000696646.1:c.*1397_*1400del	ENSP00000512777.1:n.*1397_*1400del
ENST00000696647.1:c.2586_2589del	ENSP00000512778.1:p.Lys863IlefsTer12
ENST00000696648.1:c.*611_*614del	ENSP00000512779.1:n.*611_*614del
ENST00000696649.1:c.2430_2433del	ENSP00000512780.1:p.Lys811IlefsTer12
ENST00000696650.1:n.2534_2537del
ENST00000696659.1:c.584_587del
ENST00000696663.1:c.1403_1406del
ENST00000696664.1:c.1403_1406del
ENST00000696675.1:c.2586_2589del	ENSP00000512799.1:p.Lys863IlefsTer12
ENST00000696683.1:c.1403_1406del
ENST00000696684.1:c.1403_1406del
ENST00000696685.1:c.1403_1406del
ENST00000267430.10:c.2586_2589del MANE Select	ENSP00000267430.5:p.Lys863IlefsTer12
ENST00000267430.9:c.2586_2589del	ENSP00000267430.5:p.Lys863IlefsTer12
ENST00000542564.6:c.2508_2511del	ENSP00000442493.2:p.Lys837IlefsTer12
ENST00000556250.5:c.1134_1137del	ENSP00000452033.1:p.Lys379IlefsTer12
NM_001308133.1:c.2508_2511del	NP_001295062.1:p.Lys837IlefsTer12
NM_020937.2:c.2586_2589del , LRG_502t1:c.2586_2589del	NP_065988.1:p.Lys863IlefsTer12
NM_020937.3:c.2586_2589del	NP_065988.1:p.Lys863IlefsTer12
XM_011537034.1:c.2586_2589del	XP_011535336.1:p.Lys863IlefsTer12
XM_011537035.1:c.2508_2511del	XP_011535337.1:p.Lys837IlefsTer12
XM_011537036.1:c.2586_2589del	XP_011535338.1:p.Lys863IlefsTer12
XM_011537037.1:c.600_603del	XP_011535339.1:p.Lys201IlefsTer12
XM_011537034.2:c.2586_2589del	XP_011535336.1:p.Lys863IlefsTer12
XM_011537035.3:c.2508_2511del	XP_011535337.1:p.Lys837IlefsTer12
XM_011537037.3:c.600_603del	XP_011535339.1:p.Lys201IlefsTer12
XM_017021523.1:c.2586_2589del	XP_016877012.1:p.Lys863IlefsTer12
XM_017021524.2:c.1623_1626del	XP_016877013.1:p.Lys542IlefsTer12
XM_017021525.2:c.1401_1404del	XP_016877014.1:p.Lys468IlefsTer12
XM_017021526.2:c.1401_1404del	XP_016877015.1:p.Lys468IlefsTer12
XM_017021527.1:c.1401_1404del	XP_016877016.1:p.Lys468IlefsTer12
XR_001750470.1:n.2678_2681del
XR_001750471.2:n.2678_2681del
XR_001750472.1:n.2678_2681del
NM_020937.4:c.2586_2589del MANE Select	NP_065988.1:p.Lys863IlefsTer12
NM_001308133.2:c.2508_2511del	NP_001295062.1:p.Lys837IlefsTer12