Canonical Allele Identifier: CA397485338
Community Standard Title: NM_000135.4(FANCA):c.3733C>T (p.Gln1245Ter)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89742832G>A , CM000678.2:g.89742832G>A GRCh38
NC_000016.9:g.89809240G>A , CM000678.1:g.89809240G>A GRCh37
NC_000016.8:g.88336741G>A NCBI36
NG_011706.1:g.78826C>T , LRG_495:g.78826C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.3733C>T MANE Select NP_000126.2:p.Gln1245Ter
ENST00000389301.8:c.3733C>T MANE Select ENSP00000373952.3:p.Gln1245Ter
NM_000135.2:c.3733C>T , LRG_495t1:c.3733C>T NP_000126.2:p.Gln1245Ter
NM_000135.3:c.3733C>T NP_000126.2:p.Gln1245Ter
NM_001286167.1:c.3733C>T NP_001273096.1:p.Gln1245Ter
NM_001286167.2:c.3733C>T NP_001273096.1:p.Gln1245Ter
NM_001286167.3:c.3733C>T NP_001273096.1:p.Gln1245Ter
ENST00000305699.15:n.976C>T
ENST00000389301.7:c.3733C>T ENSP00000373952.3:p.Gln1245Ter
ENST00000561667.2:c.*2211C>T ENSP00000512522.1:n.*2211C>T
ENST00000564475.5:c.63C>T
ENST00000564475.6:c.3733C>T ENSP00000454977.2:p.Gln1245Ter
ENST00000564969.5:n.51-1966C>T
ENST00000567510.2:c.2303C>T ENSP00000455969.1:n.2303C>T
ENST00000567879.5:c.211C>T ENSP00000457006.1:p.Gln71Ter
ENST00000568369.5:c.3733C>T ENSP00000456829.1:p.Gln1245Ter
ENST00000568369.6:c.3733C>T ENSP00000456829.1:p.Gln1245Ter
ENST00000568626.1:c.475-1966C>T
ENST00000696274.1:n.3694C>T
ENST00000696275.1:c.*2968C>T ENSP00000512517.1:n.*2968C>T
ENST00000696286.1:c.3733C>T ENSP00000512523.1:p.Gln1245Ter
ENST00000696287.1:c.3604C>T ENSP00000512524.1:p.Gln1202Ter
ENST00000696291.1:c.*3165C>T ENSP00000512530.1:n.*3165C>T
XM_005256294.3:c.3733C>T XP_005256351.1:p.Gln1245Ter
XM_005256294.4:c.3733C>T XP_005256351.1:p.Gln1245Ter
XM_011522945.1:c.3604C>T XP_011521247.1:p.Gln1202Ter
XM_011522945.2:c.3604C>T XP_011521247.1:p.Gln1202Ter
XM_011522946.1:c.2710C>T XP_011521248.1:p.Gln904Ter
XM_011522946.3:c.2710C>T XP_011521248.1:p.Gln904Ter
XM_011522947.1:c.2710C>T XP_011521249.1:p.Gln904Ter
XM_011522947.2:c.2710C>T XP_011521249.1:p.Gln904Ter
XM_017023044.2:c.3604C>T XP_016878533.1:p.Gln1202Ter
XM_024450189.1:c.2710C>T XP_024305957.1:p.Gln904Ter
XR_001751866.1:n.3603C>T
XR_933244.1:n.3776C>T
XR_933244.2:n.3776C>T
XR_933245.1:n.3670-1966C>T
XR_933245.2:n.3670-1966C>T
XR_933246.1:n.3603C>T