Canonical Allele Identifier: CA2241896367
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89745056G= , CM000678.2:g.89745056G= GRCh38
NC_000016.9:g.89811464G= , CM000678.1:g.89811464G= GRCh37
NC_000016.8:g.88338965G= NCBI36
NG_011706.1:g.76602C= , LRG_495:g.76602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.*2007C= ENSP00000512522.1:n.*2007C=
ENST00000564475.6:c.3529C= ENSP00000454977.2:p.Leu1177=
ENST00000567510.2:c.2099C= ENSP00000455969.1:n.2099C=
ENST00000568369.6:c.3529C= ENSP00000456829.1:p.Leu1177=
ENST00000568983.6:n.548C=
ENST00000696274.1:n.3490C=
ENST00000696275.1:c.*2764C= ENSP00000512517.1:n.*2764C=
ENST00000696286.1:c.3529C= ENSP00000512523.1:p.Leu1177=
ENST00000696287.1:c.3400C= ENSP00000512524.1:p.Leu1134=
ENST00000696291.1:c.*2961C= ENSP00000512530.1:n.*2961C=
ENST00000389301.8:c.3529C= MANE Select ENSP00000373952.3:p.Leu1177=
ENST00000305699.15:n.772C=
ENST00000389301.7:c.3529C= ENSP00000373952.3:p.Leu1177=
ENST00000561660.1:c.733C=
ENST00000567879.5:c.7C= ENSP00000457006.1:p.Leu3=
ENST00000567988.5:c.781C=
ENST00000568369.5:c.3529C= ENSP00000456829.1:p.Leu1177=
ENST00000568626.1:c.377C=
ENST00000568983.5:n.357C=
NM_000135.2:c.3529C= , LRG_495t1:c.3529C= NP_000126.2:p.Leu1177=
NM_001286167.1:c.3529C= NP_001273096.1:p.Leu1177=
XM_005256294.3:c.3529C= XP_005256351.1:p.Leu1177=
XM_011522945.1:c.3400C= XP_011521247.1:p.Leu1134=
XM_011522946.1:c.2506C= XP_011521248.1:p.Leu836=
XM_011522947.1:c.2506C= XP_011521249.1:p.Leu836=
XR_933244.1:n.3572C=
XR_933245.1:n.3572C=
XR_933246.1:n.3399C=
NM_000135.3:c.3529C= NP_000126.2:p.Leu1177=
NM_001286167.2:c.3529C= NP_001273096.1:p.Leu1177=
XM_005256294.4:c.3529C= XP_005256351.1:p.Leu1177=
XM_011522945.2:c.3400C= XP_011521247.1:p.Leu1134=
XM_011522946.3:c.2506C= XP_011521248.1:p.Leu836=
XM_011522947.2:c.2506C= XP_011521249.1:p.Leu836=
XM_017023044.2:c.3400C= XP_016878533.1:p.Leu1134=
XM_024450189.1:c.2506C= XP_024305957.1:p.Leu836=
XR_001751866.1:n.3399C=
XR_933244.2:n.3572C=
XR_933245.2:n.3572C=
NM_000135.4:c.3529C= MANE Select NP_000126.2:p.Leu1177=
NM_001286167.3:c.3529C= NP_001273096.1:p.Leu1177=