Canonical Allele Identifier: CA2635022543

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89739039-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739041_89739042del , CM000678.2:g.89739041_89739042del	GRCh38
NC_000016.9:g.89805449_89805450del , CM000678.1:g.89805449_89805450del	GRCh37
NC_000016.8:g.88332950_88332951del	NCBI36
NG_011706.1:g.82617_82618del , LRG_495:g.82617_82618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2741-67_*2741-66del (FANCA)	ENSP00000512522.1:n.*2741-67_*2741-66del
ENST00000564475.6:c.4172-67_4172-66del (FANCA)	ENSP00000454977.2:n.4172-67_4172-66del
ENST00000567510.2:c.2742-67_2742-66del (FANCA)	ENSP00000455969.1:n.2742-67_2742-66del
ENST00000568369.6:c.4172-67_4172-66del (FANCA)	ENSP00000456829.1:n.4172-67_4172-66del
ENST00000696274.1:n.4129-67_4129-66del (FANCA)
ENST00000696275.1:c.*3407-67_*3407-66del (FANCA)	ENSP00000512517.1:n.*3407-67_*3407-66del
ENST00000696286.1:c.*81-67_*81-66del (FANCA)	ENSP00000512523.1:n.*81-67_*81-66del
ENST00000696287.1:c.4043-67_4043-66del (FANCA)	ENSP00000512524.1:n.4043-67_4043-66del
ENST00000696291.1:c.*3600-67_*3600-66del (FANCA)	ENSP00000512530.1:n.*3600-67_*3600-66del
ENST00000389301.8:c.4168-67_4168-66del (FANCA) MANE Select	ENSP00000373952.3:n.4168-67_4168-66del
ENST00000443381.7:c.*795_*796del (ZNF276) MANE Select	ENSP00000415836.2:n.*795_*796del
ENST00000289816.9:c.*795_*796del (ZNF276)	ENSP00000289816.5:n.*795_*796del
ENST00000389301.7:c.4168-67_4168-66del (FANCA)	ENSP00000373952.3:n.4168-67_4168-66del
ENST00000561722.5:c.410_411del (FANCA)	ENSP00000456608.1:p.Tyr137TrpfsTer27
ENST00000562424.1:n.439-67_439-66del (FANCA)
ENST00000563983.5:n.2628_2629del (ZNF276)
ENST00000564475.5:c.502-67_502-66del (FANCA)
ENST00000564870.1:c.369-67_369-66del (FANCA)
ENST00000567879.5:c.542-67_542-66del (FANCA)	ENSP00000457006.1:n.542-67_542-66del
ENST00000568369.5:c.4172-67_4172-66del (FANCA)	ENSP00000456829.1:n.4172-67_4172-66del
NM_000135.2:c.4168-67_4168-66del , LRG_495t1:c.4168-67_4168-66del (FANCA)	NP_000126.2:n.4168-67_4168-66del
NM_001113525.1:c.*795_*796del (ZNF276)	NP_001106997.1:n.*795_*796del
NM_001286167.1:c.4172-67_4172-66del (FANCA)	NP_001273096.1:n.4172-67_4172-66del
NM_152287.3:c.*795_*796del (ZNF276)	NP_689500.2:n.*795_*796del
NR_110122.1:n.2812_2813del (ZNF276)
NR_110126.1:n.2695_2696del (ZNF276)
NR_110128.1:n.2618_2619del (ZNF276)
NR_110129.1:n.2707_2708del (ZNF276)
XM_005256294.3:c.4172-67_4172-66del (FANCA)	XP_005256351.1:n.4172-67_4172-66del
XM_011522945.1:c.4043-67_4043-66del (FANCA)	XP_011521247.1:n.4043-67_4043-66del
XM_011522946.1:c.3149-67_3149-66del (FANCA)	XP_011521248.1:n.3149-67_3149-66del
XM_011522947.1:c.3149-67_3149-66del (FANCA)	XP_011521249.1:n.3149-67_3149-66del
XR_933244.1:n.4135-67_4135-66del (FANCA)
XR_933245.1:n.4072-67_4072-66del (FANCA)
NM_000135.3:c.4168-67_4168-66del (FANCA)	NP_000126.2:n.4168-67_4168-66del
NM_001286167.2:c.4172-67_4172-66del (FANCA)	NP_001273096.1:n.4172-67_4172-66del
XM_005256294.4:c.4172-67_4172-66del (FANCA)	XP_005256351.1:n.4172-67_4172-66del
XM_011522945.2:c.4043-67_4043-66del (FANCA)	XP_011521247.1:n.4043-67_4043-66del
XM_011522946.3:c.3149-67_3149-66del (FANCA)	XP_011521248.1:n.3149-67_3149-66del
XM_011522947.2:c.3149-67_3149-66del (FANCA)	XP_011521249.1:n.3149-67_3149-66del
XM_017023044.2:c.4039-67_4039-66del (FANCA)	XP_016878533.1:n.4039-67_4039-66del
XM_017023890.1:c.*795_*796del (ZNF276)	XP_016879379.1:n.*795_*796del
XM_024450189.1:c.3149-67_3149-66del (FANCA)	XP_024305957.1:n.3149-67_3149-66del
XR_933244.2:n.4135-67_4135-66del (FANCA)
XR_933245.2:n.4072-67_4072-66del (FANCA)
XR_933484.2:n.2806_2807del (ZNF276)
NM_000135.4:c.4168-67_4168-66del (FANCA) MANE Select	NP_000126.2:n.4168-67_4168-66del
NM_001113525.2:c.*795_*796del (ZNF276) MANE Select	NP_001106997.1:n.*795_*796del
NM_001286167.3:c.4172-67_4172-66del (FANCA)	NP_001273096.1:n.4172-67_4172-66del
NM_152287.4:c.*795_*796del (ZNF276)	NP_689500.2:n.*795_*796del
NR_110122.2:n.2795_2796del (ZNF276)
NR_110126.2:n.2678_2679del (ZNF276)
NR_110129.2:n.2712_2713del (ZNF276)
NR_110128.2:n.2618_2619del (ZNF276)