Canonical Allele Identifier: CA251896
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1599
ClinVar RCV Id: RCV000001666

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45178957_45181510del , CM000676.2:g.45178957_45181510del GRCh38
NC_000014.8:g.45648160_45650713del , CM000676.1:g.45648160_45650713del GRCh37
NC_000014.7:g.44717910_44720463del NCBI36
NG_007417.1:g.48025_50578del , LRG_502:g.48025_50578del

Transcript Alleles

HGVS Amino-acid change
ENST00000554809.6:c.2434+1981_2515del
ENST00000556250.6:c.4015+1981_4096del
ENST00000696642.1:c.*3033+1981_*3114del
ENST00000696647.1:c.4222+1981_4303del
ENST00000696648.1:c.*2247+1981_*2328del
ENST00000696649.1:c.4066+1981_4147del
ENST00000696650.1:n.4170+1981_4251del
ENST00000696659.1:c.2220+1981_2301del
ENST00000696663.1:c.3040-1666_3234del
ENST00000696664.1:c.3039+1981_3120del
ENST00000696675.1:c.4274+757_*59del
ENST00000696683.1:c.3039+1981_3120del
ENST00000696684.1:c.3039+1981_3120del
ENST00000696685.1:c.3039+1981_3120del
ENST00000267430.10:c.4222+1981_4303del
ENST00000267430.9:c.4222+1981_4303del
ENST00000542564.6:c.4144+1981_4225del
ENST00000554809.5:c.1019+1981_1100del
ENST00000556250.5:c.2770+1981_2851del
NM_001308133.1:c.4144+1981_4225del
NM_020937.2:c.4222+1981_4303del , LRG_502t1:c.4222+1981_4303del
NM_020937.3:c.4222+1981_4303del
XM_011537034.1:c.4222+1981_4303del
XM_011537035.1:c.4144+1981_4225del
XM_011537036.1:c.4222+1981_4303del
XM_011537037.1:c.2236+1981_2317del
XM_011537034.2:c.4222+1981_4303del
XM_011537035.3:c.4144+1981_4225del
XM_011537037.3:c.2236+1981_2317del
XM_017021523.1:c.4222+1981_4303del
XM_017021524.2:c.3259+1981_3340del
XM_017021525.2:c.3037+1981_3118del
XM_017021526.2:c.3037+1981_3118del
XM_017021527.1:c.3037+1981_3118del
XR_001750470.1:n.4314+1981_4395del
XR_001750471.2:n.4314+1981_4395del
XR_001750472.1:n.4366+757_4447del
NM_020937.4:c.4222+1981_4303del
NM_001308133.2:c.4144+1981_4225del