Canonical Allele Identifier: CA2241889872

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739542C= , CM000678.2:g.89739542C=	GRCh38
NC_000016.9:g.89805950C= , CM000678.1:g.89805950C=	GRCh37
NC_000016.8:g.88333451C=	NCBI36
NG_011706.1:g.82116G= , LRG_495:g.82116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2519G= (FANCA)	ENSP00000512522.1:n.*2519G=
ENST00000564475.6:c.3946G= (FANCA)	ENSP00000454977.2:p.Gly1316=
ENST00000567510.2:c.2516G= (FANCA)	ENSP00000455969.1:n.2516G=
ENST00000568369.6:c.3946G= (FANCA)	ENSP00000456829.1:p.Gly1316=
ENST00000696274.1:n.3907G= (FANCA)
ENST00000696275.1:c.*3181G= (FANCA)	ENSP00000512517.1:n.*3181G=
ENST00000696286.1:c.3935-253G= (FANCA)	ENSP00000512523.1:n.3935-253G=
ENST00000696287.1:c.3817G= (FANCA)	ENSP00000512524.1:p.Gly1273=
ENST00000696291.1:c.*3378G= (FANCA)	ENSP00000512530.1:n.*3378G=
ENST00000389301.8:c.3946G= (FANCA) MANE Select	ENSP00000373952.3:p.Gly1316=
ENST00000443381.7:c.*1296C= (ZNF276) MANE Select	ENSP00000415836.2:n.*1296C=
ENST00000289816.9:c.*1296C= (ZNF276)	ENSP00000289816.5:n.*1296C=
ENST00000389301.7:c.3946G= (FANCA)	ENSP00000373952.3:p.Gly1316=
ENST00000561722.5:c.97G= (FANCA)	ENSP00000456608.1:p.Gly33=
ENST00000562424.1:n.217G= (FANCA)
ENST00000563983.5:n.3129C= (ZNF276)
ENST00000564475.5:c.276G= (FANCA)
ENST00000564870.1:c.147G= (FANCA)
ENST00000564969.5:n.671G= (FANCA)
ENST00000567879.5:c.413-276G= (FANCA)	ENSP00000457006.1:n.413-276G=
ENST00000568369.5:c.3946G= (FANCA)	ENSP00000456829.1:p.Gly1316=
ENST00000568626.1:c.655G= (FANCA)
NM_000135.2:c.3946G= , LRG_495t1:c.3946G= (FANCA)	NP_000126.2:p.Gly1316=
NM_001113525.1:c.*1296C= (ZNF276)	NP_001106997.1:n.*1296C=
NM_001286167.1:c.3946G= (FANCA)	NP_001273096.1:p.Gly1316=
NM_152287.3:c.*1296C= (ZNF276)	NP_689500.2:n.*1296C=
NR_110122.1:n.3313C= (ZNF276)
NR_110126.1:n.3196C= (ZNF276)
NR_110128.1:n.3119C= (ZNF276)
NR_110129.1:n.3208C= (ZNF276)
XM_005256294.3:c.3946G= (FANCA)	XP_005256351.1:p.Gly1316=
XM_011522945.1:c.3817G= (FANCA)	XP_011521247.1:p.Gly1273=
XM_011522946.1:c.2923G= (FANCA)	XP_011521248.1:p.Gly975=
XM_011522947.1:c.2923G= (FANCA)	XP_011521249.1:p.Gly975=
XR_933244.1:n.3978-253G= (FANCA)
XR_933245.1:n.3850G= (FANCA)
NM_000135.3:c.3946G= (FANCA)	NP_000126.2:p.Gly1316=
NM_001286167.2:c.3946G= (FANCA)	NP_001273096.1:p.Gly1316=
XM_005256294.4:c.3946G= (FANCA)	XP_005256351.1:p.Gly1316=
XM_011522945.2:c.3817G= (FANCA)	XP_011521247.1:p.Gly1273=
XM_011522946.3:c.2923G= (FANCA)	XP_011521248.1:p.Gly975=
XM_011522947.2:c.2923G= (FANCA)	XP_011521249.1:p.Gly975=
XM_017023044.2:c.3817G= (FANCA)	XP_016878533.1:p.Gly1273=
XM_017023890.1:c.*1296C= (ZNF276)	XP_016879379.1:n.*1296C=
XM_024450189.1:c.2923G= (FANCA)	XP_024305957.1:p.Gly975=
XR_001751866.1:n.3816G= (FANCA)
XR_933244.2:n.3978-253G= (FANCA)
XR_933245.2:n.3850G= (FANCA)
XR_933484.2:n.3307C= (ZNF276)
NM_000135.4:c.3946G= (FANCA) MANE Select	NP_000126.2:p.Gly1316=
NM_001113525.2:c.*1296C= (ZNF276) MANE Select	NP_001106997.1:n.*1296C=
NM_001286167.3:c.3946G= (FANCA)	NP_001273096.1:p.Gly1316=
NM_152287.4:c.*1296C= (ZNF276)	NP_689500.2:n.*1296C=
NR_110122.2:n.3296C= (ZNF276)
NR_110126.2:n.3179C= (ZNF276)
NR_110129.2:n.3213C= (ZNF276)
NR_110128.2:n.3119C= (ZNF276)