Canonical Allele Identifier: CA2635022348

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89739021-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739022_89739023del , CM000678.2:g.89739022_89739023del	GRCh38
NC_000016.9:g.89805430_89805431del , CM000678.1:g.89805430_89805431del	GRCh37
NC_000016.8:g.88332931_88332932del	NCBI36
NG_011706.1:g.82635_82636del , LRG_495:g.82635_82636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2741-49_*2741-48del (FANCA)	ENSP00000512522.1:n.*2741-49_*2741-48del
ENST00000564475.6:c.4172-49_4172-48del (FANCA)	ENSP00000454977.2:n.4172-49_4172-48del
ENST00000567510.2:c.2742-49_2742-48del (FANCA)	ENSP00000455969.1:n.2742-49_2742-48del
ENST00000568369.6:c.4172-49_4172-48del (FANCA)	ENSP00000456829.1:n.4172-49_4172-48del
ENST00000696274.1:n.4129-49_4129-48del (FANCA)
ENST00000696275.1:c.*3407-49_*3407-48del (FANCA)	ENSP00000512517.1:n.*3407-49_*3407-48del
ENST00000696286.1:c.*81-49_*81-48del (FANCA)	ENSP00000512523.1:n.*81-49_*81-48del
ENST00000696287.1:c.4043-49_4043-48del (FANCA)	ENSP00000512524.1:n.4043-49_4043-48del
ENST00000696291.1:c.*3600-49_*3600-48del (FANCA)	ENSP00000512530.1:n.*3600-49_*3600-48del
ENST00000389301.8:c.4168-49_4168-48del (FANCA) MANE Select	ENSP00000373952.3:n.4168-49_4168-48del
ENST00000443381.7:c.*776_*777del (ZNF276) MANE Select	ENSP00000415836.2:n.*776_*777del
ENST00000289816.9:c.*776_*777del (ZNF276)	ENSP00000289816.5:n.*776_*777del
ENST00000389301.7:c.4168-49_4168-48del (FANCA)	ENSP00000373952.3:n.4168-49_4168-48del
ENST00000561722.5:c.428_429del (FANCA)	ENSP00000456608.1:p.Pro143ArgfsTer21
ENST00000562424.1:n.439-49_439-48del (FANCA)
ENST00000563983.5:n.2609_2610del (ZNF276)
ENST00000564475.5:c.502-49_502-48del (FANCA)
ENST00000564870.1:c.369-49_369-48del (FANCA)
ENST00000567879.5:c.542-49_542-48del (FANCA)	ENSP00000457006.1:n.542-49_542-48del
ENST00000568369.5:c.4172-49_4172-48del (FANCA)	ENSP00000456829.1:n.4172-49_4172-48del
NM_000135.2:c.4168-49_4168-48del , LRG_495t1:c.4168-49_4168-48del (FANCA)	NP_000126.2:n.4168-49_4168-48del
NM_001113525.1:c.*776_*777del (ZNF276)	NP_001106997.1:n.*776_*777del
NM_001286167.1:c.4172-49_4172-48del (FANCA)	NP_001273096.1:n.4172-49_4172-48del
NM_152287.3:c.*776_*777del (ZNF276)	NP_689500.2:n.*776_*777del
NR_110122.1:n.2793_2794del (ZNF276)
NR_110126.1:n.2676_2677del (ZNF276)
NR_110128.1:n.2599_2600del (ZNF276)
NR_110129.1:n.2688_2689del (ZNF276)
XM_005256294.3:c.4172-49_4172-48del (FANCA)	XP_005256351.1:n.4172-49_4172-48del
XM_011522945.1:c.4043-49_4043-48del (FANCA)	XP_011521247.1:n.4043-49_4043-48del
XM_011522946.1:c.3149-49_3149-48del (FANCA)	XP_011521248.1:n.3149-49_3149-48del
XM_011522947.1:c.3149-49_3149-48del (FANCA)	XP_011521249.1:n.3149-49_3149-48del
XR_933244.1:n.4135-49_4135-48del (FANCA)
XR_933245.1:n.4072-49_4072-48del (FANCA)
NM_000135.3:c.4168-49_4168-48del (FANCA)	NP_000126.2:n.4168-49_4168-48del
NM_001286167.2:c.4172-49_4172-48del (FANCA)	NP_001273096.1:n.4172-49_4172-48del
XM_005256294.4:c.4172-49_4172-48del (FANCA)	XP_005256351.1:n.4172-49_4172-48del
XM_011522945.2:c.4043-49_4043-48del (FANCA)	XP_011521247.1:n.4043-49_4043-48del
XM_011522946.3:c.3149-49_3149-48del (FANCA)	XP_011521248.1:n.3149-49_3149-48del
XM_011522947.2:c.3149-49_3149-48del (FANCA)	XP_011521249.1:n.3149-49_3149-48del
XM_017023044.2:c.4039-49_4039-48del (FANCA)	XP_016878533.1:n.4039-49_4039-48del
XM_017023890.1:c.*776_*777del (ZNF276)	XP_016879379.1:n.*776_*777del
XM_024450189.1:c.3149-49_3149-48del (FANCA)	XP_024305957.1:n.3149-49_3149-48del
XR_933244.2:n.4135-49_4135-48del (FANCA)
XR_933245.2:n.4072-49_4072-48del (FANCA)
XR_933484.2:n.2787_2788del (ZNF276)
NM_000135.4:c.4168-49_4168-48del (FANCA) MANE Select	NP_000126.2:n.4168-49_4168-48del
NM_001113525.2:c.*776_*777del (ZNF276) MANE Select	NP_001106997.1:n.*776_*777del
NM_001286167.3:c.4172-49_4172-48del (FANCA)	NP_001273096.1:n.4172-49_4172-48del
NM_152287.4:c.*776_*777del (ZNF276)	NP_689500.2:n.*776_*777del
NR_110122.2:n.2776_2777del (ZNF276)
NR_110126.2:n.2659_2660del (ZNF276)
NR_110129.2:n.2693_2694del (ZNF276)
NR_110128.2:n.2599_2600del (ZNF276)