Canonical Allele Identifier: CA2241912553
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89773323T= , CM000678.2:g.89773323T= GRCh38
NC_000016.9:g.89839731T= , CM000678.1:g.89839731T= GRCh37
NC_000016.8:g.88367232T= NCBI36
NG_011706.1:g.48335A= , LRG_495:g.48335A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.*152A= ENSP00000512522.1:n.*152A=
ENST00000564475.6:c.1962A= ENSP00000454977.2:p.Thr654=
ENST00000567205.2:c.1962A= ENSP00000457027.2:p.Thr654=
ENST00000567284.7:n.2005A=
ENST00000567510.2:c.458A= ENSP00000455969.1:n.458A=
ENST00000568369.6:c.1962A= ENSP00000456829.1:p.Thr654=
ENST00000696274.1:n.1923A=
ENST00000696275.1:c.*1197A= ENSP00000512517.1:n.*1197A=
ENST00000696276.1:n.2005A=
ENST00000696286.1:c.1962A= ENSP00000512523.1:p.Thr654=
ENST00000696287.1:c.1962A= ENSP00000512524.1:p.Thr654=
ENST00000696291.1:c.*1378A= ENSP00000512530.1:n.*1378A=
ENST00000389301.8:c.1962A= MANE Select ENSP00000373952.3:p.Thr654=
ENST00000389301.7:c.1962A= ENSP00000373952.3:p.Thr654=
ENST00000567284.6:n.186A=
ENST00000567510.1:c.458A= ENSP00000455969.1:n.458A=
ENST00000568369.5:c.1962A= ENSP00000456829.1:p.Thr654=
NM_000135.2:c.1962A= , LRG_495t1:c.1962A= NP_000126.2:p.Thr654=
NM_001286167.1:c.1962A= NP_001273096.1:p.Thr654=
XM_005256294.3:c.1962A= XP_005256351.1:p.Thr654=
XM_011522945.1:c.1962A= XP_011521247.1:p.Thr654=
XM_011522946.1:c.939A= XP_011521248.1:p.Thr313=
XM_011522947.1:c.939A= XP_011521249.1:p.Thr313=
XM_011522948.1:c.1962A= XP_011521250.1:p.Thr654=
XR_933244.1:n.2005A=
XR_933245.1:n.2005A=
XR_933246.1:n.2005A=
XR_933247.1:n.2005A=
NM_000135.3:c.1962A= NP_000126.2:p.Thr654=
NM_001286167.2:c.1962A= NP_001273096.1:p.Thr654=
XM_005256294.4:c.1962A= XP_005256351.1:p.Thr654=
XM_011522945.2:c.1962A= XP_011521247.1:p.Thr654=
XM_011522946.3:c.939A= XP_011521248.1:p.Thr313=
XM_011522947.2:c.939A= XP_011521249.1:p.Thr313=
XM_011522948.2:c.1962A= XP_011521250.1:p.Thr654=
XM_017023044.2:c.1962A= XP_016878533.1:p.Thr654=
XM_017023045.1:c.1962A= XP_016878534.1:p.Thr654=
XM_024450189.1:c.939A= XP_024305957.1:p.Thr313=
XR_001751866.1:n.2005A=
XR_933244.2:n.2005A=
XR_933245.2:n.2005A=
XR_933247.2:n.2005A=
NM_000135.4:c.1962A= MANE Select NP_000126.2:p.Thr654=
NM_001286167.3:c.1962A= NP_001273096.1:p.Thr654=