Canonical Allele Identifier: CA2635025050

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89739525-AC-A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000561667.2:c.*2535del (FANCA)	ENSP00000512522.1:n.*2535del
ENST00000564475.6:c.3962del (FANCA)	ENSP00000454977.2:p.Arg1321LeufsTer?
ENST00000567510.2:c.2532del (FANCA)	ENSP00000455969.1:n.2532del
ENST00000568369.6:c.3962del (FANCA)	ENSP00000456829.1:p.Arg1321LeufsTer?
ENST00000696274.1:n.3923del (FANCA)
ENST00000696275.1:c.*3197del (FANCA)	ENSP00000512517.1:n.*3197del
ENST00000696286.1:c.3935-237del (FANCA)	ENSP00000512523.1:n.3935-237del
ENST00000696287.1:c.3833del (FANCA)	ENSP00000512524.1:p.Arg1278LeufsTer?
ENST00000696291.1:c.*3394del (FANCA)	ENSP00000512530.1:n.*3394del
ENST00000389301.8:c.3962del (FANCA) MANE Select	ENSP00000373952.3:p.Arg1321LeufsTer?
ENST00000443381.7:c.*1280del (ZNF276) MANE Select	ENSP00000415836.2:n.*1280del
ENST00000289816.9:c.*1280del (ZNF276)	ENSP00000289816.5:n.*1280del
ENST00000389301.7:c.3962del (FANCA)	ENSP00000373952.3:p.Arg1321LeufsTer?
ENST00000561722.5:c.113del (FANCA)	ENSP00000456608.1:p.Arg38LeufsTer?
ENST00000562424.1:n.233del (FANCA)
ENST00000563983.5:n.3113del (ZNF276)
ENST00000564475.5:c.292del (FANCA)
ENST00000564870.1:c.163del (FANCA)
ENST00000564969.5:n.687del (FANCA)
ENST00000567879.5:c.413-260del (FANCA)	ENSP00000457006.1:n.413-260del
ENST00000568369.5:c.3962del (FANCA)	ENSP00000456829.1:p.Arg1321LeufsTer?
ENST00000568626.1:c.671del (FANCA)
NM_000135.2:c.3962del , LRG_495t1:c.3962del (FANCA)	NP_000126.2:p.Arg1321LeufsTer?
NM_001113525.1:c.*1280del (ZNF276)	NP_001106997.1:n.*1280del
NM_001286167.1:c.3962del (FANCA)	NP_001273096.1:p.Arg1321LeufsTer?
NM_152287.3:c.*1280del (ZNF276)	NP_689500.2:n.*1280del
NR_110122.1:n.3297del (ZNF276)
NR_110126.1:n.3180del (ZNF276)
NR_110128.1:n.3103del (ZNF276)
NR_110129.1:n.3192del (ZNF276)
XM_005256294.3:c.3962del (FANCA)	XP_005256351.1:p.Arg1321LeufsTer?
XM_011522945.1:c.3833del (FANCA)	XP_011521247.1:p.Arg1278LeufsTer?
XM_011522946.1:c.2939del (FANCA)	XP_011521248.1:p.Arg980LeufsTer?
XM_011522947.1:c.2939del (FANCA)	XP_011521249.1:p.Arg980LeufsTer?
XR_933244.1:n.3978-237del (FANCA)
XR_933245.1:n.3866del (FANCA)
NM_000135.3:c.3962del (FANCA)	NP_000126.2:p.Arg1321LeufsTer?
NM_001286167.2:c.3962del (FANCA)	NP_001273096.1:p.Arg1321LeufsTer?
XM_005256294.4:c.3962del (FANCA)	XP_005256351.1:p.Arg1321LeufsTer?
XM_011522945.2:c.3833del (FANCA)	XP_011521247.1:p.Arg1278LeufsTer?
XM_011522946.3:c.2939del (FANCA)	XP_011521248.1:p.Arg980LeufsTer?
XM_011522947.2:c.2939del (FANCA)	XP_011521249.1:p.Arg980LeufsTer?
XM_017023044.2:c.3833del (FANCA)	XP_016878533.1:p.Arg1278LeufsTer?
XM_017023890.1:c.*1280del (ZNF276)	XP_016879379.1:n.*1280del
XM_024450189.1:c.2939del (FANCA)	XP_024305957.1:p.Arg980LeufsTer?
XR_001751866.1:n.3832del (FANCA)
XR_933244.2:n.3978-237del (FANCA)
XR_933245.2:n.3866del (FANCA)
XR_933484.2:n.3291del (ZNF276)
NM_000135.4:c.3962del (FANCA) MANE Select	NP_000126.2:p.Arg1321LeufsTer?
NM_001113525.2:c.*1280del (ZNF276) MANE Select	NP_001106997.1:n.*1280del
NM_001286167.3:c.3962del (FANCA)	NP_001273096.1:p.Arg1321LeufsTer?
NM_152287.4:c.*1280del (ZNF276)	NP_689500.2:n.*1280del
NR_110122.2:n.3280del (ZNF276)
NR_110126.2:n.3163del (ZNF276)
NR_110129.2:n.3197del (ZNF276)
NR_110128.2:n.3103del (ZNF276)