Canonical Allele Identifier: CA2635022002

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89738951-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738952del , CM000678.2:g.89738952del	GRCh38
NC_000016.9:g.89805360del , CM000678.1:g.89805360del	GRCh37
NC_000016.8:g.88332861del	NCBI36
NG_011706.1:g.82706del , LRG_495:g.82706del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2763del (FANCA)	ENSP00000512522.1:n.*2763del
ENST00000564475.6:c.4194del (FANCA)	ENSP00000454977.2:p.Asn1398LysfsTer?
ENST00000567510.2:c.2764del (FANCA)	ENSP00000455969.1:n.2764del
ENST00000568369.6:c.4194del (FANCA)	ENSP00000456829.1:p.Asn1398LysfsTer?
ENST00000696274.1:n.4151del (FANCA)
ENST00000696275.1:c.*3429del (FANCA)	ENSP00000512517.1:n.*3429del
ENST00000696286.1:c.*103del (FANCA)	ENSP00000512523.1:n.*103del
ENST00000696287.1:c.4065del (FANCA)	ENSP00000512524.1:p.Asn1355LysfsTer?
ENST00000696291.1:c.*3622del (FANCA)	ENSP00000512530.1:n.*3622del
ENST00000389301.8:c.4190del (FANCA) MANE Select	ENSP00000373952.3:p.Thr1397LysfsTer10
ENST00000443381.7:c.*706del (ZNF276) MANE Select	ENSP00000415836.2:n.*706del
ENST00000289816.9:c.*706del (ZNF276)	ENSP00000289816.5:n.*706del
ENST00000389301.7:c.4190del (FANCA)	ENSP00000373952.3:p.Thr1397LysfsTer10
ENST00000561722.5:c.436-26del (FANCA)	ENSP00000456608.1:n.436-26del
ENST00000562424.1:n.461del (FANCA)
ENST00000563983.5:n.2539del (ZNF276)
ENST00000564475.5:c.524del (FANCA)
ENST00000564870.1:c.391del (FANCA)
ENST00000567879.5:c.564del (FANCA)	ENSP00000457006.1:p.Asn188LysfsTer?
ENST00000568369.5:c.4194del (FANCA)	ENSP00000456829.1:p.Asn1398LysfsTer?
NM_000135.2:c.4190del , LRG_495t1:c.4190del (FANCA)	NP_000126.2:p.Thr1397LysfsTer10
NM_001113525.1:c.*706del (ZNF276)	NP_001106997.1:n.*706del
NM_001286167.1:c.4194del (FANCA)	NP_001273096.1:p.Asn1398LysfsTer?
NM_152287.3:c.*706del (ZNF276)	NP_689500.2:n.*706del
NR_110122.1:n.2723del (ZNF276)
NR_110126.1:n.2606del (ZNF276)
NR_110128.1:n.2529del (ZNF276)
NR_110129.1:n.2618del (ZNF276)
XM_005256294.3:c.4194del (FANCA)	XP_005256351.1:p.Asn1398LysfsTer?
XM_011522945.1:c.4065del (FANCA)	XP_011521247.1:p.Asn1355LysfsTer?
XM_011522946.1:c.3171del (FANCA)	XP_011521248.1:p.Asn1057LysfsTer?
XM_011522947.1:c.3171del (FANCA)	XP_011521249.1:p.Asn1057LysfsTer?
XR_933244.1:n.4157del (FANCA)
XR_933245.1:n.4094del (FANCA)
NM_000135.3:c.4190del (FANCA)	NP_000126.2:p.Thr1397LysfsTer10
NM_001286167.2:c.4194del (FANCA)	NP_001273096.1:p.Asn1398LysfsTer?
XM_005256294.4:c.4194del (FANCA)	XP_005256351.1:p.Asn1398LysfsTer?
XM_011522945.2:c.4065del (FANCA)	XP_011521247.1:p.Asn1355LysfsTer?
XM_011522946.3:c.3171del (FANCA)	XP_011521248.1:p.Asn1057LysfsTer?
XM_011522947.2:c.3171del (FANCA)	XP_011521249.1:p.Asn1057LysfsTer?
XM_017023044.2:c.4061del (FANCA)	XP_016878533.1:p.Thr1354LysfsTer10
XM_017023890.1:c.*706del (ZNF276)	XP_016879379.1:n.*706del
XM_024450189.1:c.3171del (FANCA)	XP_024305957.1:p.Asn1057LysfsTer?
XR_933244.2:n.4157del (FANCA)
XR_933245.2:n.4094del (FANCA)
XR_933484.2:n.2717del (ZNF276)
NM_000135.4:c.4190del (FANCA) MANE Select	NP_000126.2:p.Thr1397LysfsTer10
NM_001113525.2:c.*706del (ZNF276) MANE Select	NP_001106997.1:n.*706del
NM_001286167.3:c.4194del (FANCA)	NP_001273096.1:p.Asn1398LysfsTer?
NM_152287.4:c.*706del (ZNF276)	NP_689500.2:n.*706del
NR_110122.2:n.2706del (ZNF276)
NR_110126.2:n.2589del (ZNF276)
NR_110129.2:n.2623del (ZNF276)
NR_110128.2:n.2529del (ZNF276)