Canonical Allele Identifier: CA2241889859
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89739527G= , CM000678.2:g.89739527G= GRCh38
NC_000016.9:g.89805935G= , CM000678.1:g.89805935G= GRCh37
NC_000016.8:g.88333436G= NCBI36
NG_011706.1:g.82131C= , LRG_495:g.82131C=

Transcript Alleles

HGVS Amino-acid change
ENST00000561667.2:c.*2534C= (FANCA) ENSP00000512522.1:n.*2534C=
ENST00000564475.6:c.3961C= (FANCA) ENSP00000454977.2:p.Arg1321=
ENST00000567510.2:c.2531C= (FANCA) ENSP00000455969.1:n.2531C=
ENST00000568369.6:c.3961C= (FANCA) ENSP00000456829.1:p.Arg1321=
ENST00000696274.1:n.3922C= (FANCA)
ENST00000696275.1:c.*3196C= (FANCA) ENSP00000512517.1:n.*3196C=
ENST00000696286.1:c.3935-238C= (FANCA) ENSP00000512523.1:n.3935-238C=
ENST00000696287.1:c.3832C= (FANCA) ENSP00000512524.1:p.Arg1278=
ENST00000696291.1:c.*3393C= (FANCA) ENSP00000512530.1:n.*3393C=
ENST00000389301.8:c.3961C= (FANCA) MANE Select ENSP00000373952.3:p.Arg1321=
ENST00000443381.7:c.*1281G= (ZNF276) MANE Select ENSP00000415836.2:n.*1281G=
ENST00000289816.9:c.*1281G= (ZNF276) ENSP00000289816.5:n.*1281G=
ENST00000389301.7:c.3961C= (FANCA) ENSP00000373952.3:p.Arg1321=
ENST00000561722.5:c.112C= (FANCA) ENSP00000456608.1:p.Arg38=
ENST00000562424.1:n.232C= (FANCA)
ENST00000563983.5:n.3114G= (ZNF276)
ENST00000564475.5:c.291C= (FANCA)
ENST00000564870.1:c.162C= (FANCA)
ENST00000564969.5:n.686C= (FANCA)
ENST00000567879.5:c.413-261C= (FANCA) ENSP00000457006.1:n.413-261C=
ENST00000568369.5:c.3961C= (FANCA) ENSP00000456829.1:p.Arg1321=
ENST00000568626.1:c.670C= (FANCA)
NM_000135.2:c.3961C= , LRG_495t1:c.3961C= (FANCA) NP_000126.2:p.Arg1321=
NM_001113525.1:c.*1281G= (ZNF276) NP_001106997.1:n.*1281G=
NM_001286167.1:c.3961C= (FANCA) NP_001273096.1:p.Arg1321=
NM_152287.3:c.*1281G= (ZNF276) NP_689500.2:n.*1281G=
NR_110122.1:n.3298G= (ZNF276)
NR_110126.1:n.3181G= (ZNF276)
NR_110128.1:n.3104G= (ZNF276)
NR_110129.1:n.3193G= (ZNF276)
XM_005256294.3:c.3961C= (FANCA) XP_005256351.1:p.Arg1321=
XM_011522945.1:c.3832C= (FANCA) XP_011521247.1:p.Arg1278=
XM_011522946.1:c.2938C= (FANCA) XP_011521248.1:p.Arg980=
XM_011522947.1:c.2938C= (FANCA) XP_011521249.1:p.Arg980=
XR_933244.1:n.3978-238C= (FANCA)
XR_933245.1:n.3865C= (FANCA)
NM_000135.3:c.3961C= (FANCA) NP_000126.2:p.Arg1321=
NM_001286167.2:c.3961C= (FANCA) NP_001273096.1:p.Arg1321=
XM_005256294.4:c.3961C= (FANCA) XP_005256351.1:p.Arg1321=
XM_011522945.2:c.3832C= (FANCA) XP_011521247.1:p.Arg1278=
XM_011522946.3:c.2938C= (FANCA) XP_011521248.1:p.Arg980=
XM_011522947.2:c.2938C= (FANCA) XP_011521249.1:p.Arg980=
XM_017023044.2:c.3832C= (FANCA) XP_016878533.1:p.Arg1278=
XM_017023890.1:c.*1281G= (ZNF276) XP_016879379.1:n.*1281G=
XM_024450189.1:c.2938C= (FANCA) XP_024305957.1:p.Arg980=
XR_001751866.1:n.3831C= (FANCA)
XR_933244.2:n.3978-238C= (FANCA)
XR_933245.2:n.3865C= (FANCA)
XR_933484.2:n.3292G= (ZNF276)
NM_000135.4:c.3961C= (FANCA) MANE Select NP_000126.2:p.Arg1321=
NM_001113525.2:c.*1281G= (ZNF276) MANE Select NP_001106997.1:n.*1281G=
NM_001286167.3:c.3961C= (FANCA) NP_001273096.1:p.Arg1321=
NM_152287.4:c.*1281G= (ZNF276) NP_689500.2:n.*1281G=
NR_110122.2:n.3281G= (ZNF276)
NR_110126.2:n.3164G= (ZNF276)
NR_110129.2:n.3198G= (ZNF276)
NR_110128.2:n.3104G= (ZNF276)