Canonical Allele Identifier: CA397486715
Community Standard Title: NM_000135.4(FANCA):c.3091C>T (p.Gln1031Ter)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89749878G>A , CM000678.2:g.89749878G>A GRCh38
NC_000016.9:g.89816286G>A , CM000678.1:g.89816286G>A GRCh37
NC_000016.8:g.88343787G>A NCBI36
NG_011706.1:g.71780C>T , LRG_495:g.71780C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.3091C>T MANE Select NP_000126.2:p.Gln1031Ter
ENST00000389301.8:c.3091C>T MANE Select ENSP00000373952.3:p.Gln1031Ter
NM_000135.2:c.3091C>T , LRG_495t1:c.3091C>T NP_000126.2:p.Gln1031Ter
NM_000135.3:c.3091C>T NP_000126.2:p.Gln1031Ter
NM_001286167.1:c.3091C>T NP_001273096.1:p.Gln1031Ter
NM_001286167.2:c.3091C>T NP_001273096.1:p.Gln1031Ter
NM_001286167.3:c.3091C>T NP_001273096.1:p.Gln1031Ter
ENST00000305699.15:n.334C>T
ENST00000389301.7:c.3091C>T ENSP00000373952.3:p.Gln1031Ter
ENST00000561660.1:c.444-1111C>T
ENST00000561667.2:c.*1569C>T ENSP00000512522.1:n.*1569C>T
ENST00000563510.5:c.481C>T
ENST00000564475.6:c.3091C>T ENSP00000454977.2:p.Gln1031Ter
ENST00000567510.2:c.1661C>T ENSP00000455969.1:n.1661C>T
ENST00000567988.5:c.343C>T
ENST00000568369.5:c.3091C>T ENSP00000456829.1:p.Gln1031Ter
ENST00000568369.6:c.3091C>T ENSP00000456829.1:p.Gln1031Ter
ENST00000568983.6:n.110C>T
ENST00000696274.1:n.3052C>T
ENST00000696275.1:c.*2326C>T ENSP00000512517.1:n.*2326C>T
ENST00000696286.1:c.3091C>T ENSP00000512523.1:p.Gln1031Ter
ENST00000696287.1:c.2962C>T ENSP00000512524.1:p.Gln988Ter
ENST00000696291.1:c.*2523C>T ENSP00000512530.1:n.*2523C>T
XM_005256294.3:c.3091C>T XP_005256351.1:p.Gln1031Ter
XM_005256294.4:c.3091C>T XP_005256351.1:p.Gln1031Ter
XM_011522945.1:c.2962C>T XP_011521247.1:p.Gln988Ter
XM_011522945.2:c.2962C>T XP_011521247.1:p.Gln988Ter
XM_011522946.1:c.2068C>T XP_011521248.1:p.Gln690Ter
XM_011522946.3:c.2068C>T XP_011521248.1:p.Gln690Ter
XM_011522947.1:c.2068C>T XP_011521249.1:p.Gln690Ter
XM_011522947.2:c.2068C>T XP_011521249.1:p.Gln690Ter
XM_017023044.2:c.2962C>T XP_016878533.1:p.Gln988Ter
XM_024450189.1:c.2068C>T XP_024305957.1:p.Gln690Ter
XR_001751866.1:n.3110-1111C>T
XR_933244.1:n.3134C>T
XR_933244.2:n.3134C>T
XR_933245.1:n.3134C>T
XR_933245.2:n.3134C>T
XR_933246.1:n.3110-1111C>T