Canonical Allele Identifier: CA2241889857
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89739526C= , CM000678.2:g.89739526C= GRCh38
NC_000016.9:g.89805934C= , CM000678.1:g.89805934C= GRCh37
NC_000016.8:g.88333435C= NCBI36
NG_011706.1:g.82132G= , LRG_495:g.82132G=

Transcript Alleles

HGVS Amino-acid change
ENST00000561667.2:c.*2535G= (FANCA) ENSP00000512522.1:n.*2535G=
ENST00000564475.6:c.3962G= (FANCA) ENSP00000454977.2:p.Arg1321=
ENST00000567510.2:c.2532G= (FANCA) ENSP00000455969.1:n.2532G=
ENST00000568369.6:c.3962G= (FANCA) ENSP00000456829.1:p.Arg1321=
ENST00000696274.1:n.3923G= (FANCA)
ENST00000696275.1:c.*3197G= (FANCA) ENSP00000512517.1:n.*3197G=
ENST00000696286.1:c.3935-237G= (FANCA) ENSP00000512523.1:n.3935-237G=
ENST00000696287.1:c.3833G= (FANCA) ENSP00000512524.1:p.Arg1278=
ENST00000696291.1:c.*3394G= (FANCA) ENSP00000512530.1:n.*3394G=
ENST00000389301.8:c.3962G= (FANCA) MANE Select ENSP00000373952.3:p.Arg1321=
ENST00000443381.7:c.*1280C= (ZNF276) MANE Select ENSP00000415836.2:n.*1280C=
ENST00000289816.9:c.*1280C= (ZNF276) ENSP00000289816.5:n.*1280C=
ENST00000389301.7:c.3962G= (FANCA) ENSP00000373952.3:p.Arg1321=
ENST00000561722.5:c.113G= (FANCA) ENSP00000456608.1:p.Arg38=
ENST00000562424.1:n.233G= (FANCA)
ENST00000563983.5:n.3113C= (ZNF276)
ENST00000564475.5:c.292G= (FANCA)
ENST00000564870.1:c.163G= (FANCA)
ENST00000564969.5:n.687G= (FANCA)
ENST00000567879.5:c.413-260G= (FANCA) ENSP00000457006.1:n.413-260G=
ENST00000568369.5:c.3962G= (FANCA) ENSP00000456829.1:p.Arg1321=
ENST00000568626.1:c.671G= (FANCA)
NM_000135.2:c.3962G= , LRG_495t1:c.3962G= (FANCA) NP_000126.2:p.Arg1321=
NM_001113525.1:c.*1280C= (ZNF276) NP_001106997.1:n.*1280C=
NM_001286167.1:c.3962G= (FANCA) NP_001273096.1:p.Arg1321=
NM_152287.3:c.*1280C= (ZNF276) NP_689500.2:n.*1280C=
NR_110122.1:n.3297C= (ZNF276)
NR_110126.1:n.3180C= (ZNF276)
NR_110128.1:n.3103C= (ZNF276)
NR_110129.1:n.3192C= (ZNF276)
XM_005256294.3:c.3962G= (FANCA) XP_005256351.1:p.Arg1321=
XM_011522945.1:c.3833G= (FANCA) XP_011521247.1:p.Arg1278=
XM_011522946.1:c.2939G= (FANCA) XP_011521248.1:p.Arg980=
XM_011522947.1:c.2939G= (FANCA) XP_011521249.1:p.Arg980=
XR_933244.1:n.3978-237G= (FANCA)
XR_933245.1:n.3866G= (FANCA)
NM_000135.3:c.3962G= (FANCA) NP_000126.2:p.Arg1321=
NM_001286167.2:c.3962G= (FANCA) NP_001273096.1:p.Arg1321=
XM_005256294.4:c.3962G= (FANCA) XP_005256351.1:p.Arg1321=
XM_011522945.2:c.3833G= (FANCA) XP_011521247.1:p.Arg1278=
XM_011522946.3:c.2939G= (FANCA) XP_011521248.1:p.Arg980=
XM_011522947.2:c.2939G= (FANCA) XP_011521249.1:p.Arg980=
XM_017023044.2:c.3833G= (FANCA) XP_016878533.1:p.Arg1278=
XM_017023890.1:c.*1280C= (ZNF276) XP_016879379.1:n.*1280C=
XM_024450189.1:c.2939G= (FANCA) XP_024305957.1:p.Arg980=
XR_001751866.1:n.3832G= (FANCA)
XR_933244.2:n.3978-237G= (FANCA)
XR_933245.2:n.3866G= (FANCA)
XR_933484.2:n.3291C= (ZNF276)
NM_000135.4:c.3962G= (FANCA) MANE Select NP_000126.2:p.Arg1321=
NM_001113525.2:c.*1280C= (ZNF276) MANE Select NP_001106997.1:n.*1280C=
NM_001286167.3:c.3962G= (FANCA) NP_001273096.1:p.Arg1321=
NM_152287.4:c.*1280C= (ZNF276) NP_689500.2:n.*1280C=
NR_110122.2:n.3280C= (ZNF276)
NR_110126.2:n.3163C= (ZNF276)
NR_110129.2:n.3197C= (ZNF276)
NR_110128.2:n.3103C= (ZNF276)