Canonical Allele Identifier: CA2241896348
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89745050G= , CM000678.2:g.89745050G= GRCh38
NC_000016.9:g.89811458G= , CM000678.1:g.89811458G= GRCh37
NC_000016.8:g.88338959G= NCBI36
NG_011706.1:g.76608C= , LRG_495:g.76608C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.*2013C= ENSP00000512522.1:n.*2013C=
ENST00000564475.6:c.3535C= ENSP00000454977.2:p.Pro1179=
ENST00000567510.2:c.2105C= ENSP00000455969.1:n.2105C=
ENST00000568369.6:c.3535C= ENSP00000456829.1:p.Pro1179=
ENST00000568983.6:n.554C=
ENST00000696274.1:n.3496C=
ENST00000696275.1:c.*2770C= ENSP00000512517.1:n.*2770C=
ENST00000696286.1:c.3535C= ENSP00000512523.1:p.Pro1179=
ENST00000696287.1:c.3406C= ENSP00000512524.1:p.Pro1136=
ENST00000696291.1:c.*2967C= ENSP00000512530.1:n.*2967C=
ENST00000389301.8:c.3535C= MANE Select ENSP00000373952.3:p.Pro1179=
ENST00000305699.15:n.778C=
ENST00000389301.7:c.3535C= ENSP00000373952.3:p.Pro1179=
ENST00000561660.1:c.739C=
ENST00000567879.5:c.13C= ENSP00000457006.1:p.Pro5=
ENST00000567988.5:c.787C=
ENST00000568369.5:c.3535C= ENSP00000456829.1:p.Pro1179=
ENST00000568626.1:c.383C=
ENST00000568983.5:n.363C=
NM_000135.2:c.3535C= , LRG_495t1:c.3535C= NP_000126.2:p.Pro1179=
NM_001286167.1:c.3535C= NP_001273096.1:p.Pro1179=
XM_005256294.3:c.3535C= XP_005256351.1:p.Pro1179=
XM_011522945.1:c.3406C= XP_011521247.1:p.Pro1136=
XM_011522946.1:c.2512C= XP_011521248.1:p.Pro838=
XM_011522947.1:c.2512C= XP_011521249.1:p.Pro838=
XR_933244.1:n.3578C=
XR_933245.1:n.3578C=
XR_933246.1:n.3405C=
NM_000135.3:c.3535C= NP_000126.2:p.Pro1179=
NM_001286167.2:c.3535C= NP_001273096.1:p.Pro1179=
XM_005256294.4:c.3535C= XP_005256351.1:p.Pro1179=
XM_011522945.2:c.3406C= XP_011521247.1:p.Pro1136=
XM_011522946.3:c.2512C= XP_011521248.1:p.Pro838=
XM_011522947.2:c.2512C= XP_011521249.1:p.Pro838=
XM_017023044.2:c.3406C= XP_016878533.1:p.Pro1136=
XM_024450189.1:c.2512C= XP_024305957.1:p.Pro838=
XR_001751866.1:n.3405C=
XR_933244.2:n.3578C=
XR_933245.2:n.3578C=
NM_000135.4:c.3535C= MANE Select NP_000126.2:p.Pro1179=
NM_001286167.3:c.3535C= NP_001273096.1:p.Pro1179=