Canonical Allele Identifier: CA2241889527
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89739058_89739059delinsCG , CM000678.2:g.89739058_89739059delinsCG GRCh38
NC_000016.9:g.89805466_89805467delinsCG , CM000678.1:g.89805466_89805467delinsCG GRCh37
NC_000016.8:g.88332967_88332968delinsCG NCBI36
NG_011706.1:g.82599_82600delinsCG , LRG_495:g.82599_82600delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561667.2:c.*2740+74_*2740+75delinsCG (FANCA) ENSP00000512522.1:n.*2740+74_*2740+75delinsCG
ENST00000564475.6:c.4171+70_4171+71delinsCG (FANCA) ENSP00000454977.2:n.4171+70_4171+71delinsCG
ENST00000567510.2:c.2741+70_2741+71delinsCG (FANCA) ENSP00000455969.1:n.2741+70_2741+71delinsCG
ENST00000568369.6:c.4171+70_4171+71delinsCG (FANCA) ENSP00000456829.1:n.4171+70_4171+71delinsCG
ENST00000696274.1:n.4128+74_4128+75delinsCG (FANCA)
ENST00000696275.1:c.*3406+70_*3406+71delinsCG (FANCA) ENSP00000512517.1:n.*3406+70_*3406+71delinsCG
ENST00000696286.1:c.*80+74_*80+75delinsCG (FANCA) ENSP00000512523.1:n.*80+74_*80+75delinsCG
ENST00000696287.1:c.4042+70_4042+71delinsCG (FANCA) ENSP00000512524.1:n.4042+70_4042+71delinsCG
ENST00000696291.1:c.*3599+74_*3599+75delinsCG (FANCA) ENSP00000512530.1:n.*3599+74_*3599+75delinsCG
ENST00000389301.8:c.4167+74_4167+75delinsCG (FANCA) MANE Select ENSP00000373952.3:n.4167+74_4167+75delinsCG
ENST00000443381.7:c.*812_*813delinsCG (ZNF276) MANE Select ENSP00000415836.2:n.*812_*813delinsCG
ENST00000289816.9:c.*812_*813delinsCG (ZNF276) ENSP00000289816.5:n.*812_*813delinsCG
ENST00000389301.7:c.4167+74_4167+75delinsCG (FANCA) ENSP00000373952.3:n.4167+74_4167+75delinsCG
ENST00000561722.5:c.392_393delinsCG (FANCA) ENSP00000456608.1:p.Pro131=
ENST00000562424.1:n.438+74_438+75delinsCG (FANCA)
ENST00000563983.5:n.2645_2646delinsCG (ZNF276)
ENST00000564475.5:c.501+70_501+71delinsCG (FANCA)
ENST00000564870.1:c.368+74_368+75delinsCG (FANCA)
ENST00000567879.5:c.541+79_541+80delinsCG (FANCA) ENSP00000457006.1:n.541+79_541+80delinsCG
ENST00000568369.5:c.4171+70_4171+71delinsCG (FANCA) ENSP00000456829.1:n.4171+70_4171+71delinsCG
NM_000135.2:c.4167+74_4167+75delinsCG , LRG_495t1:c.4167+74_4167+75delinsCG (FANCA) NP_000126.2:n.4167+74_4167+75delinsCG
NM_001113525.1:c.*812_*813delinsCG (ZNF276) NP_001106997.1:n.*812_*813delinsCG
NM_001286167.1:c.4171+70_4171+71delinsCG (FANCA) NP_001273096.1:n.4171+70_4171+71delinsCG
NM_152287.3:c.*812_*813delinsCG (ZNF276) NP_689500.2:n.*812_*813delinsCG
NR_110122.1:n.2829_2830delinsCG (ZNF276)
NR_110126.1:n.2712_2713delinsCG (ZNF276)
NR_110128.1:n.2635_2636delinsCG (ZNF276)
NR_110129.1:n.2724_2725delinsCG (ZNF276)
XM_005256294.3:c.4171+70_4171+71delinsCG (FANCA) XP_005256351.1:n.4171+70_4171+71delinsCG
XM_011522945.1:c.4042+70_4042+71delinsCG (FANCA) XP_011521247.1:n.4042+70_4042+71delinsCG
XM_011522946.1:c.3148+70_3148+71delinsCG (FANCA) XP_011521248.1:n.3148+70_3148+71delinsCG
XM_011522947.1:c.3148+70_3148+71delinsCG (FANCA) XP_011521249.1:n.3148+70_3148+71delinsCG
XR_933244.1:n.4134+74_4134+75delinsCG (FANCA)
XR_933245.1:n.4071+74_4071+75delinsCG (FANCA)
NM_000135.3:c.4167+74_4167+75delinsCG (FANCA) NP_000126.2:n.4167+74_4167+75delinsCG
NM_001286167.2:c.4171+70_4171+71delinsCG (FANCA) NP_001273096.1:n.4171+70_4171+71delinsCG
XM_005256294.4:c.4171+70_4171+71delinsCG (FANCA) XP_005256351.1:n.4171+70_4171+71delinsCG
XM_011522945.2:c.4042+70_4042+71delinsCG (FANCA) XP_011521247.1:n.4042+70_4042+71delinsCG
XM_011522946.3:c.3148+70_3148+71delinsCG (FANCA) XP_011521248.1:n.3148+70_3148+71delinsCG
XM_011522947.2:c.3148+70_3148+71delinsCG (FANCA) XP_011521249.1:n.3148+70_3148+71delinsCG
XM_017023044.2:c.4038+74_4038+75delinsCG (FANCA) XP_016878533.1:n.4038+74_4038+75delinsCG
XM_017023890.1:c.*812_*813delinsCG (ZNF276) XP_016879379.1:n.*812_*813delinsCG
XM_024450189.1:c.3148+70_3148+71delinsCG (FANCA) XP_024305957.1:n.3148+70_3148+71delinsCG
XR_933244.2:n.4134+74_4134+75delinsCG (FANCA)
XR_933245.2:n.4071+74_4071+75delinsCG (FANCA)
XR_933484.2:n.2823_2824delinsCG (ZNF276)
NM_000135.4:c.4167+74_4167+75delinsCG (FANCA) MANE Select NP_000126.2:n.4167+74_4167+75delinsCG
NM_001113525.2:c.*812_*813delinsCG (ZNF276) MANE Select NP_001106997.1:n.*812_*813delinsCG
NM_001286167.3:c.4171+70_4171+71delinsCG (FANCA) NP_001273096.1:n.4171+70_4171+71delinsCG
NM_152287.4:c.*812_*813delinsCG (ZNF276) NP_689500.2:n.*812_*813delinsCG
NR_110122.2:n.2812_2813delinsCG (ZNF276)
NR_110126.2:n.2695_2696delinsCG (ZNF276)
NR_110129.2:n.2729_2730delinsCG (ZNF276)
NR_110128.2:n.2635_2636delinsCG (ZNF276)
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