Canonical Allele Identifier: CA2831039577
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89739126_89739142del , CM000678.2:g.89739126_89739142del GRCh38
NC_000016.9:g.89805534_89805550del , CM000678.1:g.89805534_89805550del GRCh37
NC_000016.8:g.88333035_88333051del NCBI36
NG_011706.1:g.82522_82538del , LRG_495:g.82522_82538del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.*2737_*2740+13del (FANCA)
ENST00000564475.6:c.4164_4171+9del (FANCA)
ENST00000567510.2:c.2734_2741+9del (FANCA)
ENST00000568369.6:c.4164_4171+9del (FANCA)
ENST00000696274.1:n.4125_4128+13del (FANCA)
ENST00000696275.1:c.*3399_*3406+9del (FANCA)
ENST00000696286.1:c.*77_*80+13del (FANCA)
ENST00000696287.1:c.4035_4042+9del (FANCA)
ENST00000696291.1:c.*3596_*3599+13del (FANCA)
ENST00000389301.8:c.4164_4167+13del (FANCA)
ENST00000443381.7:c.*880_*896del (ZNF276) MANE Select ENSP00000415836.2:n.*880_*896del
ENST00000289816.9:c.*880_*896del (ZNF276) ENSP00000289816.5:n.*880_*896del
ENST00000389301.7:c.4164_4167+13del (FANCA)
ENST00000561722.5:c.315_331del (FANCA) ENSP00000456608.1:p.Ala107SerfsTer?
ENST00000562424.1:n.435_438+13del (FANCA)
ENST00000563983.5:n.2713_2729del (ZNF276)
ENST00000564475.5:c.494_501+9del (FANCA)
ENST00000564870.1:c.365_368+13del (FANCA)
ENST00000567879.5:c.541+2_541+18del (FANCA)
ENST00000568369.5:c.4164_4171+9del (FANCA)
NM_000135.2:c.4164_4167+13del , LRG_495t1:c.4164_4167+13del (FANCA)
NM_001113525.1:c.*880_*896del (ZNF276) NP_001106997.1:n.*880_*896del
NM_001286167.1:c.4164_4171+9del (FANCA)
NM_152287.3:c.*880_*896del (ZNF276) NP_689500.2:n.*880_*896del
NR_110122.1:n.2897_2913del (ZNF276)
NR_110126.1:n.2780_2796del (ZNF276)
NR_110128.1:n.2703_2719del (ZNF276)
NR_110129.1:n.2792_2808del (ZNF276)
XM_005256294.3:c.4164_4171+9del (FANCA)
XM_011522945.1:c.4035_4042+9del (FANCA)
XM_011522946.1:c.3141_3148+9del (FANCA)
XM_011522947.1:c.3141_3148+9del (FANCA)
XR_933244.1:n.4131_4134+13del (FANCA)
XR_933245.1:n.4068_4071+13del (FANCA)
NM_000135.3:c.4164_4167+13del (FANCA)
NM_001286167.2:c.4164_4171+9del (FANCA)
XM_005256294.4:c.4164_4171+9del (FANCA)
XM_011522945.2:c.4035_4042+9del (FANCA)
XM_011522946.3:c.3141_3148+9del (FANCA)
XM_011522947.2:c.3141_3148+9del (FANCA)
XM_017023044.2:c.4035_4038+13del (FANCA)
XM_017023890.1:c.*880_*896del (ZNF276) XP_016879379.1:n.*880_*896del
XM_024450189.1:c.3141_3148+9del (FANCA)
XR_933244.2:n.4131_4134+13del (FANCA)
XR_933245.2:n.4068_4071+13del (FANCA)
XR_933484.2:n.2891_2907del (ZNF276)
NM_000135.4:c.4164_4167+13del (FANCA)
NM_001113525.2:c.*880_*896del (ZNF276) MANE Select NP_001106997.1:n.*880_*896del
NM_001286167.3:c.4164_4171+9del (FANCA)
NM_152287.4:c.*880_*896del (ZNF276) NP_689500.2:n.*880_*896del
NR_110122.2:n.2880_2896del (ZNF276)
NR_110126.2:n.2763_2779del (ZNF276)
NR_110129.2:n.2797_2813del (ZNF276)
NR_110128.2:n.2703_2719del (ZNF276)