Canonical Allele Identifier: CA16615029
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408180
ClinVar RCV Id: RCV000475930
dbSNP Id: rs1060501878
MyVariant Identifiers: chr16:g.89839712T>A (hg19) chr16:g.89773304T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89773304T>A , CM000678.2:g.89773304T>A GRCh38
NC_000016.9:g.89839712T>A , CM000678.1:g.89839712T>A GRCh37
NC_000016.8:g.88367213T>A NCBI36
NG_011706.1:g.48354A>T , LRG_495:g.48354A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000561667.2:c.*171A>T ENSP00000512522.1:n.*171A>T
ENST00000564475.6:c.1981A>T ENSP00000454977.2:p.Arg661Ter
ENST00000567205.2:c.1981A>T ENSP00000457027.2:p.Arg661Ter
ENST00000567284.7:n.2024A>T
ENST00000567510.2:c.477A>T ENSP00000455969.1:n.477A>T
ENST00000568369.6:c.1981A>T ENSP00000456829.1:p.Arg661Ter
ENST00000696274.1:n.1942A>T
ENST00000696275.1:c.*1216A>T ENSP00000512517.1:n.*1216A>T
ENST00000696276.1:n.2024A>T
ENST00000696286.1:c.1981A>T ENSP00000512523.1:p.Arg661Ter
ENST00000696287.1:c.1981A>T ENSP00000512524.1:p.Arg661Ter
ENST00000696291.1:c.*1397A>T ENSP00000512530.1:n.*1397A>T
ENST00000389301.8:c.1981A>T MANE Select ENSP00000373952.3:p.Arg661Ter
ENST00000389301.7:c.1981A>T ENSP00000373952.3:p.Arg661Ter
ENST00000567284.6:n.205A>T
ENST00000568369.5:c.1981A>T ENSP00000456829.1:p.Arg661Ter
NM_000135.2:c.1981A>T , LRG_495t1:c.1981A>T NP_000126.2:p.Arg661Ter
NM_001286167.1:c.1981A>T NP_001273096.1:p.Arg661Ter
XM_005256294.3:c.1981A>T XP_005256351.1:p.Arg661Ter
XM_011522945.1:c.1981A>T XP_011521247.1:p.Arg661Ter
XM_011522946.1:c.958A>T XP_011521248.1:p.Arg320Ter
XM_011522947.1:c.958A>T XP_011521249.1:p.Arg320Ter
XM_011522948.1:c.1981A>T XP_011521250.1:p.Arg661Ter
XR_933244.1:n.2024A>T
XR_933245.1:n.2024A>T
XR_933246.1:n.2024A>T
XR_933247.1:n.2024A>T
NM_000135.3:c.1981A>T NP_000126.2:p.Arg661Ter
NM_001286167.2:c.1981A>T NP_001273096.1:p.Arg661Ter
XM_005256294.4:c.1981A>T XP_005256351.1:p.Arg661Ter
XM_011522945.2:c.1981A>T XP_011521247.1:p.Arg661Ter
XM_011522946.3:c.958A>T XP_011521248.1:p.Arg320Ter
XM_011522947.2:c.958A>T XP_011521249.1:p.Arg320Ter
XM_011522948.2:c.1981A>T XP_011521250.1:p.Arg661Ter
XM_017023044.2:c.1981A>T XP_016878533.1:p.Arg661Ter
XM_017023045.1:c.1981A>T XP_016878534.1:p.Arg661Ter
XM_024450189.1:c.958A>T XP_024305957.1:p.Arg320Ter
XR_001751866.1:n.2024A>T
XR_933244.2:n.2024A>T
XR_933245.2:n.2024A>T
XR_933247.2:n.2024A>T
NM_000135.4:c.1981A>T MANE Select NP_000126.2:p.Arg661Ter
NM_001286167.3:c.1981A>T NP_001273096.1:p.Arg661Ter
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