Canonical Allele Identifier: CA10649301
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89737589T>C , CM000678.2:g.89737589T>C GRCh38
NC_000016.9:g.89803997T>C , CM000678.1:g.89803997T>C GRCh37
NC_000016.8:g.88331498T>C NCBI36
NG_011706.1:g.84069A>G , LRG_495:g.84069A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.*1012A>G (FANCA) MANE Select NP_000126.2:n.*1012A>G
NM_001113525.2:c.1475-217T>C (ZNF276) MANE Select NP_001106997.1:n.1475-217T>C
ENST00000389301.8:c.*1012A>G (FANCA) MANE Select ENSP00000373952.3:n.*1012A>G
ENST00000443381.7:c.1475-217T>C (ZNF276) MANE Select ENSP00000415836.2:n.1475-217T>C
NM_000135.2:c.*1012A>G , LRG_495t1:c.*1012A>G (FANCA) NP_000126.2:n.*1012A>G
NM_000135.3:c.*1012A>G (FANCA) NP_000126.2:n.*1012A>G
NM_001113525.1:c.1475-217T>C (ZNF276) NP_001106997.1:n.1475-217T>C
NM_001286167.1:c.*1109A>G (FANCA) NP_001273096.1:n.*1109A>G
NM_001286167.2:c.*1109A>G (FANCA) NP_001273096.1:n.*1109A>G
NM_001286167.3:c.*1109A>G (FANCA) NP_001273096.1:n.*1109A>G
NM_152287.3:c.1250-217T>C (ZNF276) NP_689500.2:n.1250-217T>C
NM_152287.4:c.1250-217T>C (ZNF276) NP_689500.2:n.1250-217T>C
NR_110122.1:n.1562-132T>C (ZNF276)
NR_110122.2:n.1545-132T>C (ZNF276)
NR_110126.1:n.1530-217T>C (ZNF276)
NR_110126.2:n.1513-217T>C (ZNF276)
NR_110128.1:n.1453-217T>C (ZNF276)
NR_110128.2:n.1453-217T>C (ZNF276)
NR_110129.1:n.1542-217T>C (ZNF276)
NR_110129.2:n.1547-217T>C (ZNF276)
ENST00000289816.9:c.1250-217T>C (ZNF276) ENSP00000289816.5:n.1250-217T>C
ENST00000389301.7:c.*1012A>G (FANCA) ENSP00000373952.3:n.*1012A>G
ENST00000443381.6:c.1475-217T>C (ZNF276) ENSP00000415836.2:n.1475-217T>C
ENST00000561536.5:n.1234-217T>C (ZNF276)
ENST00000561667.2:c.*3472+654A>G (FANCA) ENSP00000512522.1:n.*3472+654A>G
ENST00000562530.5:c.*375-217T>C (ZNF276) ENSP00000455466.1:n.*375-217T>C
ENST00000563983.5:n.1463-217T>C (ZNF276)
ENST00000564004.5:n.2151-217T>C (ZNF276)
ENST00000568064.5:c.1199-217T>C (ZNF276) ENSP00000457210.1:n.1199-217T>C
ENST00000568295.5:c.*375-217T>C (ZNF276) ENSP00000457313.1:n.*375-217T>C
ENST00000568369.6:c.*1109A>G (FANCA) ENSP00000456829.1:n.*1109A>G
ENST00000569582.1:n.359-217T>C (ZNF276)
XM_005256324.3:c.1424-217T>C (ZNF276) XP_005256381.1:n.1424-217T>C
XM_005256328.3:c.833-217T>C (ZNF276) XP_005256385.1:n.833-217T>C
XM_006721337.1:c.1250-217T>C (ZNF276) XP_006721400.1:n.1250-217T>C
XM_011523460.1:c.1250-217T>C (ZNF276) XP_011521762.1:n.1250-217T>C
XM_017023890.1:c.833-217T>C (ZNF276) XP_016879379.1:n.833-217T>C
XR_001752030.1:n.2694-217T>C (ZNF276)
XR_001752031.1:n.1553-132T>C (ZNF276)
XR_001752032.1:n.1622-217T>C (ZNF276)
XR_002957853.1:n.2054-217T>C (ZNF276)
XR_243507.2:n.1553-217T>C (ZNF276)
XR_429740.1:n.1572-132T>C (ZNF276)
XR_429740.2:n.1572-132T>C (ZNF276)
XR_933484.2:n.1641-217T>C (ZNF276)