Canonical Allele Identifier: CA8252724
Community Standard Title: NM_000135.4(FANCA):c.837C>T (p.Asp279=)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89799222G>A , CM000678.2:g.89799222G>A GRCh38
NC_000016.9:g.89865630G>A , CM000678.1:g.89865630G>A GRCh37
NC_000016.8:g.88393131G>A NCBI36
NG_011706.1:g.22436C>T , LRG_495:g.22436C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.837C>T MANE Select NP_000126.2:p.Asp279=
ENST00000389301.8:c.837C>T MANE Select ENSP00000373952.3:p.Asp279=
NM_000135.2:c.837C>T , LRG_495t1:c.837C>T NP_000126.2:p.Asp279=
NM_000135.3:c.837C>T NP_000126.2:p.Asp279=
NM_001018112.1:c.837C>T NP_001018122.1:p.Asp279=
NM_001018112.2:c.837C>T NP_001018122.1:p.Asp279=
NM_001018112.3:c.837C>T NP_001018122.1:p.Asp279=
NM_001286167.1:c.837C>T NP_001273096.1:p.Asp279=
NM_001286167.2:c.837C>T NP_001273096.1:p.Asp279=
NM_001286167.3:c.837C>T NP_001273096.1:p.Asp279=
NM_001351830.1:c.741C>T NP_001338759.1:p.Asp247=
NM_001351830.2:c.741C>T NP_001338759.1:p.Asp247=
ENST00000389301.7:c.837C>T ENSP00000373952.3:p.Asp279=
ENST00000389302.7:c.837C>T ENSP00000373953.3:p.Asp279=
ENST00000534992.5:c.837C>T ENSP00000443675.1:p.Asp279=
ENST00000543736.5:c.741C>T ENSP00000443409.1:p.Asp247=
ENST00000561667.2:c.837C>T ENSP00000512522.1:p.Asp279=
ENST00000563673.5:c.837C>T ENSP00000456443.1:p.Asp279=
ENST00000563767.2:n.589C>T
ENST00000564475.6:c.837C>T ENSP00000454977.2:p.Asp279=
ENST00000565582.5:c.667C>T ENSP00000456722.1:n.667C>T
ENST00000566409.1:c.11C>T
ENST00000566889.5:n.1419C>T
ENST00000567205.2:c.837C>T ENSP00000457027.2:p.Asp279=
ENST00000567284.7:n.880C>T
ENST00000567621.5:c.314C>T
ENST00000567621.6:c.837C>T ENSP00000456762.2:p.Asp279=
ENST00000568369.5:c.837C>T ENSP00000456829.1:p.Asp279=
ENST00000568369.6:c.837C>T ENSP00000456829.1:p.Asp279=
ENST00000696274.1:n.911C>T
ENST00000696275.1:c.837C>T ENSP00000512517.1:p.Asp279=
ENST00000696276.1:n.880C>T
ENST00000696277.1:c.837C>T ENSP00000512518.1:p.Asp279=
ENST00000696286.1:c.837C>T ENSP00000512523.1:p.Asp279=
ENST00000696287.1:c.837C>T ENSP00000512524.1:p.Asp279=
ENST00000696288.1:c.868C>T ENSP00000512525.1:n.868C>T
ENST00000696291.1:c.*181C>T ENSP00000512530.1:n.*181C>T
ENST00000696292.1:c.702C>T ENSP00000512531.1:n.702C>T
ENST00000696293.1:c.694C>T ENSP00000512532.1:n.694C>T
ENST00000696294.1:c.672C>T ENSP00000512533.1:p.Asp224=
ENST00000696295.1:c.672C>T ENSP00000512534.1:p.Asp224=
XM_005256294.3:c.837C>T XP_005256351.1:p.Asp279=
XM_005256294.4:c.837C>T XP_005256351.1:p.Asp279=
XM_011522945.1:c.837C>T XP_011521247.1:p.Asp279=
XM_011522945.2:c.837C>T XP_011521247.1:p.Asp279=
XM_011522946.1:c.-316C>T XP_011521248.1:n.-316C>T
XM_011522946.3:c.-316C>T XP_011521248.1:n.-316C>T
XM_011522947.1:c.-74C>T XP_011521249.1:n.-74C>T
XM_011522947.2:c.-74C>T XP_011521249.1:n.-74C>T
XM_011522948.1:c.837C>T XP_011521250.1:p.Asp279=
XM_011522948.2:c.837C>T XP_011521250.1:p.Asp279=
XM_017023044.2:c.837C>T XP_016878533.1:p.Asp279=
XM_017023045.1:c.837C>T XP_016878534.1:p.Asp279=
XM_017023046.1:c.837C>T XP_016878535.1:p.Asp279=
XM_024450189.1:c.-316C>T XP_024305957.1:n.-316C>T
XR_001751866.1:n.880C>T
XR_001751867.1:n.880C>T
XR_001751868.2:n.880C>T
XR_002957793.1:n.880C>T
XR_933244.1:n.880C>T
XR_933244.2:n.880C>T
XR_933245.1:n.880C>T
XR_933245.2:n.880C>T
XR_933246.1:n.880C>T
XR_933247.1:n.880C>T
XR_933247.2:n.880C>T