Canonical Allele Identifier: CA8251157
Community Standard Title: NM_000135.4(FANCA):c.3421G>A (p.Ala1141Thr)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89746676C>T , CM000678.2:g.89746676C>T GRCh38
NC_000016.9:g.89813084C>T , CM000678.1:g.89813084C>T GRCh37
NC_000016.8:g.88340585C>T NCBI36
NG_011706.1:g.74982G>A , LRG_495:g.74982G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.3421G>A MANE Select NP_000126.2:p.Ala1141Thr
ENST00000389301.8:c.3421G>A MANE Select ENSP00000373952.3:p.Ala1141Thr
NM_000135.2:c.3421G>A , LRG_495t1:c.3421G>A NP_000126.2:p.Ala1141Thr
NM_000135.3:c.3421G>A NP_000126.2:p.Ala1141Thr
NM_001286167.1:c.3421G>A NP_001273096.1:p.Ala1141Thr
NM_001286167.2:c.3421G>A NP_001273096.1:p.Ala1141Thr
NM_001286167.3:c.3421G>A NP_001273096.1:p.Ala1141Thr
ENST00000305699.15:n.664G>A
ENST00000389301.7:c.3421G>A ENSP00000373952.3:p.Ala1141Thr
ENST00000561660.1:c.625G>A
ENST00000561667.2:c.*1899G>A ENSP00000512522.1:n.*1899G>A
ENST00000564475.6:c.3421G>A ENSP00000454977.2:p.Ala1141Thr
ENST00000567510.2:c.1991G>A ENSP00000455969.1:n.1991G>A
ENST00000567988.5:c.673G>A
ENST00000568369.5:c.3421G>A ENSP00000456829.1:p.Ala1141Thr
ENST00000568369.6:c.3421G>A ENSP00000456829.1:p.Ala1141Thr
ENST00000568626.1:c.269G>A
ENST00000568983.5:n.249G>A
ENST00000568983.6:n.440G>A
ENST00000696274.1:n.3382G>A
ENST00000696275.1:c.*2656G>A ENSP00000512517.1:n.*2656G>A
ENST00000696286.1:c.3421G>A ENSP00000512523.1:p.Ala1141Thr
ENST00000696287.1:c.3292G>A ENSP00000512524.1:p.Ala1098Thr
ENST00000696291.1:c.*2853G>A ENSP00000512530.1:n.*2853G>A
XM_005256294.3:c.3421G>A XP_005256351.1:p.Ala1141Thr
XM_005256294.4:c.3421G>A XP_005256351.1:p.Ala1141Thr
XM_011522945.1:c.3292G>A XP_011521247.1:p.Ala1098Thr
XM_011522945.2:c.3292G>A XP_011521247.1:p.Ala1098Thr
XM_011522946.1:c.2398G>A XP_011521248.1:p.Ala800Thr
XM_011522946.3:c.2398G>A XP_011521248.1:p.Ala800Thr
XM_011522947.1:c.2398G>A XP_011521249.1:p.Ala800Thr
XM_011522947.2:c.2398G>A XP_011521249.1:p.Ala800Thr
XM_017023044.2:c.3292G>A XP_016878533.1:p.Ala1098Thr
XM_024450189.1:c.2398G>A XP_024305957.1:p.Ala800Thr
XR_001751866.1:n.3291G>A
XR_933244.1:n.3464G>A
XR_933244.2:n.3464G>A
XR_933245.1:n.3464G>A
XR_933245.2:n.3464G>A
XR_933246.1:n.3291G>A