Canonical Allele Identifier: CA159337

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739506T>C , CM000678.2:g.89739506T>C	GRCh38
NC_000016.9:g.89805914T>C , CM000678.1:g.89805914T>C	GRCh37
NC_000016.8:g.88333415T>C	NCBI36
NG_011706.1:g.82152A>G , LRG_495:g.82152A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.3982A>G (FANCA) MANE Select	NP_000126.2:p.Thr1328Ala
NM_001113525.2:c.*1260T>C (ZNF276) MANE Select	NP_001106997.1:n.*1260T>C
ENST00000389301.8:c.3982A>G (FANCA) MANE Select	ENSP00000373952.3:p.Thr1328Ala
ENST00000443381.7:c.*1260T>C (ZNF276) MANE Select	ENSP00000415836.2:n.*1260T>C
NM_000135.2:c.3982A>G , LRG_495t1:c.3982A>G (FANCA)	NP_000126.2:p.Thr1328Ala
NM_000135.3:c.3982A>G (FANCA)	NP_000126.2:p.Thr1328Ala
NM_001113525.1:c.*1260T>C (ZNF276)	NP_001106997.1:n.*1260T>C
NM_001286167.1:c.3982A>G (FANCA)	NP_001273096.1:p.Thr1328Ala
NM_001286167.2:c.3982A>G (FANCA)	NP_001273096.1:p.Thr1328Ala
NM_001286167.3:c.3982A>G (FANCA)	NP_001273096.1:p.Thr1328Ala
NM_152287.3:c.*1260T>C (ZNF276)	NP_689500.2:n.*1260T>C
NM_152287.4:c.*1260T>C (ZNF276)	NP_689500.2:n.*1260T>C
NR_110122.1:n.3277T>C (ZNF276)
NR_110122.2:n.3260T>C (ZNF276)
NR_110126.1:n.3160T>C (ZNF276)
NR_110126.2:n.3143T>C (ZNF276)
NR_110128.1:n.3083T>C (ZNF276)
NR_110128.2:n.3083T>C (ZNF276)
NR_110129.1:n.3172T>C (ZNF276)
NR_110129.2:n.3177T>C (ZNF276)
ENST00000289816.9:c.*1260T>C (ZNF276)	ENSP00000289816.5:n.*1260T>C
ENST00000389301.7:c.3982A>G (FANCA)	ENSP00000373952.3:p.Thr1328Ala
ENST00000561667.2:c.*2555A>G (FANCA)	ENSP00000512522.1:n.*2555A>G
ENST00000561722.5:c.133A>G (FANCA)	ENSP00000456608.1:p.Thr45Ala
ENST00000562424.1:n.253A>G (FANCA)
ENST00000563983.5:n.3093T>C (ZNF276)
ENST00000564475.5:c.312A>G (FANCA)
ENST00000564475.6:c.3982A>G (FANCA)	ENSP00000454977.2:p.Thr1328Ala
ENST00000564870.1:c.183A>G (FANCA)
ENST00000564969.5:n.707A>G (FANCA)
ENST00000567510.2:c.2552A>G (FANCA)	ENSP00000455969.1:n.2552A>G
ENST00000567879.5:c.413-240A>G (FANCA)	ENSP00000457006.1:n.413-240A>G
ENST00000568369.5:c.3982A>G (FANCA)	ENSP00000456829.1:p.Thr1328Ala
ENST00000568369.6:c.3982A>G (FANCA)	ENSP00000456829.1:p.Thr1328Ala
ENST00000568626.1:c.691A>G (FANCA)
ENST00000696274.1:n.3943A>G (FANCA)
ENST00000696275.1:c.*3217A>G (FANCA)	ENSP00000512517.1:n.*3217A>G
ENST00000696286.1:c.3935-217A>G (FANCA)	ENSP00000512523.1:n.3935-217A>G
ENST00000696287.1:c.3853A>G (FANCA)	ENSP00000512524.1:p.Thr1285Ala
ENST00000696291.1:c.*3414A>G (FANCA)	ENSP00000512530.1:n.*3414A>G
XM_005256294.3:c.3982A>G (FANCA)	XP_005256351.1:p.Thr1328Ala
XM_005256294.4:c.3982A>G (FANCA)	XP_005256351.1:p.Thr1328Ala
XM_011522945.1:c.3853A>G (FANCA)	XP_011521247.1:p.Thr1285Ala
XM_011522945.2:c.3853A>G (FANCA)	XP_011521247.1:p.Thr1285Ala
XM_011522946.1:c.2959A>G (FANCA)	XP_011521248.1:p.Thr987Ala
XM_011522946.3:c.2959A>G (FANCA)	XP_011521248.1:p.Thr987Ala
XM_011522947.1:c.2959A>G (FANCA)	XP_011521249.1:p.Thr987Ala
XM_011522947.2:c.2959A>G (FANCA)	XP_011521249.1:p.Thr987Ala
XM_017023044.2:c.3853A>G (FANCA)	XP_016878533.1:p.Thr1285Ala
XM_017023890.1:c.*1260T>C (ZNF276)	XP_016879379.1:n.*1260T>C
XM_024450189.1:c.2959A>G (FANCA)	XP_024305957.1:p.Thr987Ala
XR_001751866.1:n.3852A>G (FANCA)
XR_933244.1:n.3978-217A>G (FANCA)
XR_933244.2:n.3978-217A>G (FANCA)
XR_933245.1:n.3886A>G (FANCA)
XR_933245.2:n.3886A>G (FANCA)
XR_933484.2:n.3271T>C (ZNF276)