Canonical Allele Identifier: CA1139664991
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 974088
ClinVar RCV Id: RCV001256329
dbSNP Id: rs2040861554

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89811072del , CM000678.2:g.89811072del GRCh38
NC_000016.9:g.89877480del , CM000678.1:g.89877480del GRCh37
NC_000016.8:g.88404981del NCBI36
NG_011706.1:g.10587del , LRG_495:g.10587del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.284del
ENST00000563767.2:n.119del
ENST00000564475.6:c.284del
ENST00000567205.2:c.284del
ENST00000567284.7:n.327del
ENST00000567621.6:c.284del
ENST00000568369.6:c.284del
ENST00000696275.1:c.284del
ENST00000696276.1:n.327del
ENST00000696277.1:c.284del
ENST00000696286.1:c.284del
ENST00000696287.1:c.284del
ENST00000696288.1:c.315del
ENST00000696291.1:c.284del
ENST00000696292.1:c.149del ENSP00000512531.1:n.149del
ENST00000696293.1:c.141del
ENST00000696294.1:c.119del
ENST00000696295.1:c.119del
ENST00000696296.1:c.119del
ENST00000389301.8:c.284del
ENST00000389301.7:c.284del
ENST00000389302.7:c.284del
ENST00000534992.5:c.284del
ENST00000543736.5:c.284del
ENST00000563513.1:c.284-14del ENSP00000455946.1:n.284-14del
ENST00000563673.5:c.284del
ENST00000565582.5:c.197del
ENST00000566889.5:n.866del
ENST00000567883.5:n.277del
ENST00000567943.1:c.*264del
ENST00000568369.5:c.284del
NM_000135.2:c.284del , LRG_495t1:c.284del
NM_001018112.1:c.284del
NM_001286167.1:c.284del
XM_005256294.3:c.284del
XM_011522945.1:c.284del
XM_011522948.1:c.284del
XR_933244.1:n.327del
XR_933245.1:n.327del
XR_933246.1:n.327del
XR_933247.1:n.327del
NM_000135.3:c.284del
NM_001018112.2:c.284del
NM_001286167.2:c.284del
NM_001351830.1:c.284del
XM_005256294.4:c.284del
XM_011522945.2:c.284del
XM_011522946.3:c.-869del
XM_011522948.2:c.284del
XM_017023044.2:c.284del
XM_017023045.1:c.284del
XM_017023046.1:c.284del
XR_001751866.1:n.327del
XR_001751867.1:n.327del
XR_001751868.2:n.327del
XR_002957793.1:n.327del
XR_933244.2:n.327del
XR_933245.2:n.327del
XR_933247.2:n.327del
NM_000135.4:c.284del
NM_001018112.3:c.284del
NM_001286167.3:c.284del
NM_001351830.2:c.284del