Canonical Allele Identifier: CA2241889495

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739011_89739017delinsCATACAG , CM000678.2:g.89739011_89739017delinsCATACAG	GRCh38
NC_000016.9:g.89805419_89805425delinsCATACAG , CM000678.1:g.89805419_89805425delinsCATACAG	GRCh37
NC_000016.8:g.88332920_88332926delinsCATACAG	NCBI36
NG_011706.1:g.82641_82647delinsCTGTATG , LRG_495:g.82641_82647delinsCTGTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2741-43_*2741-37delinsCTGTATG (FANCA)	ENSP00000512522.1:n.*2741-43_*2741-37delinsCTGTATG
ENST00000564475.6:c.4172-43_4172-37delinsCTGTATG (FANCA)	ENSP00000454977.2:n.4172-43_4172-37delinsCTGTATG
ENST00000567510.2:c.2742-43_2742-37delinsCTGTATG (FANCA)	ENSP00000455969.1:n.2742-43_2742-37delinsCTGTATG
ENST00000568369.6:c.4172-43_4172-37delinsCTGTATG (FANCA)	ENSP00000456829.1:n.4172-43_4172-37delinsCTGTATG
ENST00000696274.1:n.4129-43_4129-37delinsCTGTATG (FANCA)
ENST00000696275.1:c.*3407-43_*3407-37delinsCTGTATG (FANCA)	ENSP00000512517.1:n.*3407-43_*3407-37delinsCTGTATG
ENST00000696286.1:c.*81-43_*81-37delinsCTGTATG (FANCA)	ENSP00000512523.1:n.*81-43_*81-37delinsCTGTATG
ENST00000696287.1:c.4043-43_4043-37delinsCTGTATG (FANCA)	ENSP00000512524.1:n.4043-43_4043-37delinsCTGTATG
ENST00000696291.1:c.*3600-43_*3600-37delinsCTGTATG (FANCA)	ENSP00000512530.1:n.*3600-43_*3600-37delinsCTGTATG
ENST00000389301.8:c.4168-43_4168-37delinsCTGTATG (FANCA) MANE Select	ENSP00000373952.3:n.4168-43_4168-37delinsCTGTATG
ENST00000443381.7:c.*765_*771delinsCATACAG (ZNF276) MANE Select	ENSP00000415836.2:n.*765_*771delinsCATACAG
ENST00000289816.9:c.*765_*771delinsCATACAG (ZNF276)	ENSP00000289816.5:n.*765_*771delinsCATACAG
ENST00000389301.7:c.4168-43_4168-37delinsCTGTATG (FANCA)	ENSP00000373952.3:n.4168-43_4168-37delinsCTGTATG
ENST00000561722.5:c.434_435+5delinsCTGTATG (FANCA)
ENST00000562424.1:n.439-43_439-37delinsCTGTATG (FANCA)
ENST00000563983.5:n.2598_2604delinsCATACAG (ZNF276)
ENST00000564475.5:c.502-43_502-37delinsCTGTATG (FANCA)
ENST00000564870.1:c.369-43_369-37delinsCTGTATG (FANCA)
ENST00000567879.5:c.542-43_542-37delinsCTGTATG (FANCA)	ENSP00000457006.1:n.542-43_542-37delinsCTGTATG
ENST00000568369.5:c.4172-43_4172-37delinsCTGTATG (FANCA)	ENSP00000456829.1:n.4172-43_4172-37delinsCTGTATG
NM_000135.2:c.4168-43_4168-37delinsCTGTATG , LRG_495t1:c.4168-43_4168-37delinsCTGTATG (FANCA)	NP_000126.2:n.4168-43_4168-37delinsCTGTATG
NM_001113525.1:c.*765_*771delinsCATACAG (ZNF276)	NP_001106997.1:n.*765_*771delinsCATACAG
NM_001286167.1:c.4172-43_4172-37delinsCTGTATG (FANCA)	NP_001273096.1:n.4172-43_4172-37delinsCTGTATG
NM_152287.3:c.*765_*771delinsCATACAG (ZNF276)	NP_689500.2:n.*765_*771delinsCATACAG
NR_110122.1:n.2782_2788delinsCATACAG (ZNF276)
NR_110126.1:n.2665_2671delinsCATACAG (ZNF276)
NR_110128.1:n.2588_2594delinsCATACAG (ZNF276)
NR_110129.1:n.2677_2683delinsCATACAG (ZNF276)
XM_005256294.3:c.4172-43_4172-37delinsCTGTATG (FANCA)	XP_005256351.1:n.4172-43_4172-37delinsCTGTATG
XM_011522945.1:c.4043-43_4043-37delinsCTGTATG (FANCA)	XP_011521247.1:n.4043-43_4043-37delinsCTGTATG
XM_011522946.1:c.3149-43_3149-37delinsCTGTATG (FANCA)	XP_011521248.1:n.3149-43_3149-37delinsCTGTATG
XM_011522947.1:c.3149-43_3149-37delinsCTGTATG (FANCA)	XP_011521249.1:n.3149-43_3149-37delinsCTGTATG
XR_933244.1:n.4135-43_4135-37delinsCTGTATG (FANCA)
XR_933245.1:n.4072-43_4072-37delinsCTGTATG (FANCA)
NM_000135.3:c.4168-43_4168-37delinsCTGTATG (FANCA)	NP_000126.2:n.4168-43_4168-37delinsCTGTATG
NM_001286167.2:c.4172-43_4172-37delinsCTGTATG (FANCA)	NP_001273096.1:n.4172-43_4172-37delinsCTGTATG
XM_005256294.4:c.4172-43_4172-37delinsCTGTATG (FANCA)	XP_005256351.1:n.4172-43_4172-37delinsCTGTATG
XM_011522945.2:c.4043-43_4043-37delinsCTGTATG (FANCA)	XP_011521247.1:n.4043-43_4043-37delinsCTGTATG
XM_011522946.3:c.3149-43_3149-37delinsCTGTATG (FANCA)	XP_011521248.1:n.3149-43_3149-37delinsCTGTATG
XM_011522947.2:c.3149-43_3149-37delinsCTGTATG (FANCA)	XP_011521249.1:n.3149-43_3149-37delinsCTGTATG
XM_017023044.2:c.4039-43_4039-37delinsCTGTATG (FANCA)	XP_016878533.1:n.4039-43_4039-37delinsCTGTATG
XM_017023890.1:c.*765_*771delinsCATACAG (ZNF276)	XP_016879379.1:n.*765_*771delinsCATACAG
XM_024450189.1:c.3149-43_3149-37delinsCTGTATG (FANCA)	XP_024305957.1:n.3149-43_3149-37delinsCTGTATG
XR_933244.2:n.4135-43_4135-37delinsCTGTATG (FANCA)
XR_933245.2:n.4072-43_4072-37delinsCTGTATG (FANCA)
XR_933484.2:n.2776_2782delinsCATACAG (ZNF276)
NM_000135.4:c.4168-43_4168-37delinsCTGTATG (FANCA) MANE Select	NP_000126.2:n.4168-43_4168-37delinsCTGTATG
NM_001113525.2:c.*765_*771delinsCATACAG (ZNF276) MANE Select	NP_001106997.1:n.*765_*771delinsCATACAG
NM_001286167.3:c.4172-43_4172-37delinsCTGTATG (FANCA)	NP_001273096.1:n.4172-43_4172-37delinsCTGTATG
NM_152287.4:c.*765_*771delinsCATACAG (ZNF276)	NP_689500.2:n.*765_*771delinsCATACAG
NR_110122.2:n.2765_2771delinsCATACAG (ZNF276)
NR_110126.2:n.2648_2654delinsCATACAG (ZNF276)
NR_110129.2:n.2682_2688delinsCATACAG (ZNF276)
NR_110128.2:n.2588_2594delinsCATACAG (ZNF276)