Canonical Allele Identifier: CA397485887

Gene: FANCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89746619G>A , CM000678.2:g.89746619G>A	GRCh38
NC_000016.9:g.89813027G>A , CM000678.1:g.89813027G>A	GRCh37
NC_000016.8:g.88340528G>A	NCBI36
NG_011706.1:g.75039C>T , LRG_495:g.75039C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*1956C>T	ENSP00000512522.1:n.*1956C>T
ENST00000564475.6:c.3478C>T	ENSP00000454977.2:p.Gln1160Ter
ENST00000567510.2:c.2048C>T	ENSP00000455969.1:n.2048C>T
ENST00000568369.6:c.3478C>T	ENSP00000456829.1:p.Gln1160Ter
ENST00000568983.6:n.497C>T
ENST00000696274.1:n.3439C>T
ENST00000696275.1:c.*2713C>T	ENSP00000512517.1:n.*2713C>T
ENST00000696286.1:c.3478C>T	ENSP00000512523.1:p.Gln1160Ter
ENST00000696287.1:c.3349C>T	ENSP00000512524.1:p.Gln1117Ter
ENST00000696291.1:c.*2910C>T	ENSP00000512530.1:n.*2910C>T
ENST00000389301.8:c.3478C>T MANE Select	ENSP00000373952.3:p.Gln1160Ter
ENST00000305699.15:n.721C>T
ENST00000389301.7:c.3478C>T	ENSP00000373952.3:p.Gln1160Ter
ENST00000561660.1:c.682C>T
ENST00000567988.5:c.730C>T
ENST00000568369.5:c.3478C>T	ENSP00000456829.1:p.Gln1160Ter
ENST00000568626.1:c.326C>T
ENST00000568983.5:n.306C>T
NM_000135.2:c.3478C>T , LRG_495t1:c.3478C>T	NP_000126.2:p.Gln1160Ter
NM_001286167.1:c.3478C>T	NP_001273096.1:p.Gln1160Ter
XM_005256294.3:c.3478C>T	XP_005256351.1:p.Gln1160Ter
XM_011522945.1:c.3349C>T	XP_011521247.1:p.Gln1117Ter
XM_011522946.1:c.2455C>T	XP_011521248.1:p.Gln819Ter
XM_011522947.1:c.2455C>T	XP_011521249.1:p.Gln819Ter
XR_933244.1:n.3521C>T
XR_933245.1:n.3521C>T
XR_933246.1:n.3348C>T
NM_000135.3:c.3478C>T	NP_000126.2:p.Gln1160Ter
NM_001286167.2:c.3478C>T	NP_001273096.1:p.Gln1160Ter
XM_005256294.4:c.3478C>T	XP_005256351.1:p.Gln1160Ter
XM_011522945.2:c.3349C>T	XP_011521247.1:p.Gln1117Ter
XM_011522946.3:c.2455C>T	XP_011521248.1:p.Gln819Ter
XM_011522947.2:c.2455C>T	XP_011521249.1:p.Gln819Ter
XM_017023044.2:c.3349C>T	XP_016878533.1:p.Gln1117Ter
XM_024450189.1:c.2455C>T	XP_024305957.1:p.Gln819Ter
XR_001751866.1:n.3348C>T
XR_933244.2:n.3521C>T
XR_933245.2:n.3521C>T
NM_000135.4:c.3478C>T MANE Select	NP_000126.2:p.Gln1160Ter
NM_001286167.3:c.3478C>T	NP_001273096.1:p.Gln1160Ter