Canonical Allele Identifier: CA912996778

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805934_89805937del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739526_89739529del , CM000678.2:g.89739526_89739529del	GRCh38
NC_000016.9:g.89805934_89805937del , CM000678.1:g.89805934_89805937del	GRCh37
NC_000016.8:g.88333435_88333438del	NCBI36
NG_011706.1:g.82130_82133del , LRG_495:g.82130_82133del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561667.2:c.*2533_*2536del (FANCA)	ENSP00000512522.1:n.*2533_*2536del
ENST00000564475.6:c.3960_3963del (FANCA)	ENSP00000454977.2:p.Arg1321TrpfsTer?
ENST00000567510.2:c.2530_2533del (FANCA)	ENSP00000455969.1:n.2530_2533del
ENST00000568369.6:c.3960_3963del (FANCA)	ENSP00000456829.1:p.Arg1321TrpfsTer?
ENST00000696274.1:n.3921_3924del (FANCA)
ENST00000696275.1:c.*3195_*3198del (FANCA)	ENSP00000512517.1:n.*3195_*3198del
ENST00000696286.1:c.3935-239_3935-236del (FANCA)	ENSP00000512523.1:n.3935-239_3935-236del
ENST00000696287.1:c.3831_3834del (FANCA)	ENSP00000512524.1:p.Arg1278TrpfsTer?
ENST00000696291.1:c.*3392_*3395del (FANCA)	ENSP00000512530.1:n.*3392_*3395del
ENST00000389301.8:c.3960_3963del (FANCA) MANE Select	ENSP00000373952.3:p.Arg1321TrpfsTer?
ENST00000443381.7:c.*1280_*1283del (ZNF276) MANE Select	ENSP00000415836.2:n.*1280_*1283del
ENST00000289816.9:c.*1280_*1283del (ZNF276)	ENSP00000289816.5:n.*1280_*1283del
ENST00000389301.7:c.3960_3963del (FANCA)	ENSP00000373952.3:p.Arg1321TrpfsTer?
ENST00000561722.5:c.111_114del (FANCA)	ENSP00000456608.1:p.Arg38TrpfsTer?
ENST00000562424.1:n.231_234del (FANCA)
ENST00000563983.5:n.3113_3116del (ZNF276)
ENST00000564475.5:c.290_293del (FANCA)
ENST00000564870.1:c.161_164del (FANCA)
ENST00000564969.5:n.685_688del (FANCA)
ENST00000567879.5:c.413-262_413-259del (FANCA)	ENSP00000457006.1:n.413-262_413-259del
ENST00000568369.5:c.3960_3963del (FANCA)	ENSP00000456829.1:p.Arg1321TrpfsTer?
ENST00000568626.1:c.669_672del (FANCA)
NM_000135.2:c.3960_3963del , LRG_495t1:c.3960_3963del (FANCA)	NP_000126.2:p.Arg1321TrpfsTer?
NM_001113525.1:c.*1280_*1283del (ZNF276)	NP_001106997.1:n.*1280_*1283del
NM_001286167.1:c.3960_3963del (FANCA)	NP_001273096.1:p.Arg1321TrpfsTer?
NM_152287.3:c.*1280_*1283del (ZNF276)	NP_689500.2:n.*1280_*1283del
NR_110122.1:n.3297_3300del (ZNF276)
NR_110126.1:n.3180_3183del (ZNF276)
NR_110128.1:n.3103_3106del (ZNF276)
NR_110129.1:n.3192_3195del (ZNF276)
XM_005256294.3:c.3960_3963del (FANCA)	XP_005256351.1:p.Arg1321TrpfsTer?
XM_011522945.1:c.3831_3834del (FANCA)	XP_011521247.1:p.Arg1278TrpfsTer?
XM_011522946.1:c.2937_2940del (FANCA)	XP_011521248.1:p.Arg980TrpfsTer?
XM_011522947.1:c.2937_2940del (FANCA)	XP_011521249.1:p.Arg980TrpfsTer?
XR_933244.1:n.3978-239_3978-236del (FANCA)
XR_933245.1:n.3864_3867del (FANCA)
NM_000135.3:c.3960_3963del (FANCA)	NP_000126.2:p.Arg1321TrpfsTer?
NM_001286167.2:c.3960_3963del (FANCA)	NP_001273096.1:p.Arg1321TrpfsTer?
XM_005256294.4:c.3960_3963del (FANCA)	XP_005256351.1:p.Arg1321TrpfsTer?
XM_011522945.2:c.3831_3834del (FANCA)	XP_011521247.1:p.Arg1278TrpfsTer?
XM_011522946.3:c.2937_2940del (FANCA)	XP_011521248.1:p.Arg980TrpfsTer?
XM_011522947.2:c.2937_2940del (FANCA)	XP_011521249.1:p.Arg980TrpfsTer?
XM_017023044.2:c.3831_3834del (FANCA)	XP_016878533.1:p.Arg1278TrpfsTer?
XM_017023890.1:c.*1280_*1283del (ZNF276)	XP_016879379.1:n.*1280_*1283del
XM_024450189.1:c.2937_2940del (FANCA)	XP_024305957.1:p.Arg980TrpfsTer?
XR_001751866.1:n.3830_3833del (FANCA)
XR_933244.2:n.3978-239_3978-236del (FANCA)
XR_933245.2:n.3864_3867del (FANCA)
XR_933484.2:n.3291_3294del (ZNF276)
NM_000135.4:c.3960_3963del (FANCA) MANE Select	NP_000126.2:p.Arg1321TrpfsTer?
NM_001113525.2:c.*1280_*1283del (ZNF276) MANE Select	NP_001106997.1:n.*1280_*1283del
NM_001286167.3:c.3960_3963del (FANCA)	NP_001273096.1:p.Arg1321TrpfsTer?
NM_152287.4:c.*1280_*1283del (ZNF276)	NP_689500.2:n.*1280_*1283del
NR_110122.2:n.3280_3283del (ZNF276)
NR_110126.2:n.3163_3166del (ZNF276)
NR_110129.2:n.3197_3200del (ZNF276)
NR_110128.2:n.3103_3106del (ZNF276)