Canonical Allele Identifier: CA397459605
Community Standard Title: NM_000135.4(FANCA):c.1464C>G (p.Tyr488Ter)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89784860G>C , CM000678.2:g.89784860G>C GRCh38
NC_000016.9:g.89851268G>C , CM000678.1:g.89851268G>C GRCh37
NC_000016.8:g.88378769G>C NCBI36
NG_011706.1:g.36798C>G , LRG_495:g.36798C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.1464C>G MANE Select NP_000126.2:p.Tyr488Ter
ENST00000389301.8:c.1464C>G MANE Select ENSP00000373952.3:p.Tyr488Ter
NM_000135.2:c.1464C>G , LRG_495t1:c.1464C>G NP_000126.2:p.Tyr488Ter
NM_000135.3:c.1464C>G NP_000126.2:p.Tyr488Ter
NM_001286167.1:c.1464C>G NP_001273096.1:p.Tyr488Ter
NM_001286167.2:c.1464C>G NP_001273096.1:p.Tyr488Ter
NM_001286167.3:c.1464C>G NP_001273096.1:p.Tyr488Ter
ENST00000389301.7:c.1464C>G ENSP00000373952.3:p.Tyr488Ter
ENST00000561667.2:c.1464C>G ENSP00000512522.1:p.Tyr488Ter
ENST00000564475.6:c.1464C>G ENSP00000454977.2:p.Tyr488Ter
ENST00000567205.2:c.1464C>G ENSP00000457027.2:p.Tyr488Ter
ENST00000567284.7:n.1507C>G
ENST00000568369.5:c.1464C>G ENSP00000456829.1:p.Tyr488Ter
ENST00000568369.6:c.1464C>G ENSP00000456829.1:p.Tyr488Ter
ENST00000696274.1:n.1425C>G
ENST00000696275.1:c.*699C>G ENSP00000512517.1:n.*699C>G
ENST00000696276.1:n.1507C>G
ENST00000696277.1:c.*105C>G ENSP00000512518.1:n.*105C>G
ENST00000696286.1:c.1464C>G ENSP00000512523.1:p.Tyr488Ter
ENST00000696287.1:c.1464C>G ENSP00000512524.1:p.Tyr488Ter
ENST00000696291.1:c.*808C>G ENSP00000512530.1:n.*808C>G
XM_005256294.3:c.1464C>G XP_005256351.1:p.Tyr488Ter
XM_005256294.4:c.1464C>G XP_005256351.1:p.Tyr488Ter
XM_011522945.1:c.1464C>G XP_011521247.1:p.Tyr488Ter
XM_011522945.2:c.1464C>G XP_011521247.1:p.Tyr488Ter
XM_011522946.1:c.441C>G XP_011521248.1:p.Tyr147Ter
XM_011522946.3:c.441C>G XP_011521248.1:p.Tyr147Ter
XM_011522947.1:c.441C>G XP_011521249.1:p.Tyr147Ter
XM_011522947.2:c.441C>G XP_011521249.1:p.Tyr147Ter
XM_011522948.1:c.1464C>G XP_011521250.1:p.Tyr488Ter
XM_011522948.2:c.1464C>G XP_011521250.1:p.Tyr488Ter
XM_017023044.2:c.1464C>G XP_016878533.1:p.Tyr488Ter
XM_017023045.1:c.1464C>G XP_016878534.1:p.Tyr488Ter
XM_017023046.1:c.*13C>G XP_016878535.1:n.*13C>G
XM_024450189.1:c.441C>G XP_024305957.1:p.Tyr147Ter
XR_001751866.1:n.1507C>G
XR_001751867.1:n.1543C>G
XR_933244.1:n.1507C>G
XR_933244.2:n.1507C>G
XR_933245.1:n.1507C>G
XR_933245.2:n.1507C>G
XR_933246.1:n.1507C>G
XR_933247.1:n.1507C>G
XR_933247.2:n.1507C>G