Canonical Allele Identifier: CA2241889483

Gene: FANCA ZNF276

Linked Data

• dbSNP Id: rs2062047942

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739002_89739006del , CM000678.2:g.89739002_89739006del	GRCh38
NC_000016.9:g.89805410_89805414del , CM000678.1:g.89805410_89805414del	GRCh37
NC_000016.8:g.88332911_88332915del	NCBI36
NG_011706.1:g.82654_82658del , LRG_495:g.82654_82658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2741-30_*2741-26del (FANCA)	ENSP00000512522.1:n.*2741-30_*2741-26del
ENST00000564475.6:c.4172-30_4172-26del (FANCA)	ENSP00000454977.2:n.4172-30_4172-26del
ENST00000567510.2:c.2742-30_2742-26del (FANCA)	ENSP00000455969.1:n.2742-30_2742-26del
ENST00000568369.6:c.4172-30_4172-26del (FANCA)	ENSP00000456829.1:n.4172-30_4172-26del
ENST00000696274.1:n.4129-30_4129-26del (FANCA)
ENST00000696275.1:c.*3407-30_*3407-26del (FANCA)	ENSP00000512517.1:n.*3407-30_*3407-26del
ENST00000696286.1:c.*81-30_*81-26del (FANCA)	ENSP00000512523.1:n.*81-30_*81-26del
ENST00000696287.1:c.4043-30_4043-26del (FANCA)	ENSP00000512524.1:n.4043-30_4043-26del
ENST00000696291.1:c.*3600-30_*3600-26del (FANCA)	ENSP00000512530.1:n.*3600-30_*3600-26del
ENST00000389301.8:c.4168-30_4168-26del (FANCA) MANE Select	ENSP00000373952.3:n.4168-30_4168-26del
ENST00000443381.7:c.*756_*760del (ZNF276) MANE Select	ENSP00000415836.2:n.*756_*760del
ENST00000289816.9:c.*756_*760del (ZNF276)	ENSP00000289816.5:n.*756_*760del
ENST00000389301.7:c.4168-30_4168-26del (FANCA)	ENSP00000373952.3:n.4168-30_4168-26del
ENST00000561722.5:c.435+12_435+16del (FANCA)	ENSP00000456608.1:n.435+12_435+16del
ENST00000562424.1:n.439-30_439-26del (FANCA)
ENST00000563983.5:n.2589_2593del (ZNF276)
ENST00000564475.5:c.502-30_502-26del (FANCA)
ENST00000564870.1:c.369-30_369-26del (FANCA)
ENST00000567879.5:c.542-30_542-26del (FANCA)	ENSP00000457006.1:n.542-30_542-26del
ENST00000568369.5:c.4172-30_4172-26del (FANCA)	ENSP00000456829.1:n.4172-30_4172-26del
NM_000135.2:c.4168-30_4168-26del , LRG_495t1:c.4168-30_4168-26del (FANCA)	NP_000126.2:n.4168-30_4168-26del
NM_001113525.1:c.*756_*760del (ZNF276)	NP_001106997.1:n.*756_*760del
NM_001286167.1:c.4172-30_4172-26del (FANCA)	NP_001273096.1:n.4172-30_4172-26del
NM_152287.3:c.*756_*760del (ZNF276)	NP_689500.2:n.*756_*760del
NR_110122.1:n.2773_2777del (ZNF276)
NR_110126.1:n.2656_2660del (ZNF276)
NR_110128.1:n.2579_2583del (ZNF276)
NR_110129.1:n.2668_2672del (ZNF276)
XM_005256294.3:c.4172-30_4172-26del (FANCA)	XP_005256351.1:n.4172-30_4172-26del
XM_011522945.1:c.4043-30_4043-26del (FANCA)	XP_011521247.1:n.4043-30_4043-26del
XM_011522946.1:c.3149-30_3149-26del (FANCA)	XP_011521248.1:n.3149-30_3149-26del
XM_011522947.1:c.3149-30_3149-26del (FANCA)	XP_011521249.1:n.3149-30_3149-26del
XR_933244.1:n.4135-30_4135-26del (FANCA)
XR_933245.1:n.4072-30_4072-26del (FANCA)
NM_000135.3:c.4168-30_4168-26del (FANCA)	NP_000126.2:n.4168-30_4168-26del
NM_001286167.2:c.4172-30_4172-26del (FANCA)	NP_001273096.1:n.4172-30_4172-26del
XM_005256294.4:c.4172-30_4172-26del (FANCA)	XP_005256351.1:n.4172-30_4172-26del
XM_011522945.2:c.4043-30_4043-26del (FANCA)	XP_011521247.1:n.4043-30_4043-26del
XM_011522946.3:c.3149-30_3149-26del (FANCA)	XP_011521248.1:n.3149-30_3149-26del
XM_011522947.2:c.3149-30_3149-26del (FANCA)	XP_011521249.1:n.3149-30_3149-26del
XM_017023044.2:c.4039-30_4039-26del (FANCA)	XP_016878533.1:n.4039-30_4039-26del
XM_017023890.1:c.*756_*760del (ZNF276)	XP_016879379.1:n.*756_*760del
XM_024450189.1:c.3149-30_3149-26del (FANCA)	XP_024305957.1:n.3149-30_3149-26del
XR_933244.2:n.4135-30_4135-26del (FANCA)
XR_933245.2:n.4072-30_4072-26del (FANCA)
XR_933484.2:n.2767_2771del (ZNF276)
NM_000135.4:c.4168-30_4168-26del (FANCA) MANE Select	NP_000126.2:n.4168-30_4168-26del
NM_001113525.2:c.*756_*760del (ZNF276) MANE Select	NP_001106997.1:n.*756_*760del
NM_001286167.3:c.4172-30_4172-26del (FANCA)	NP_001273096.1:n.4172-30_4172-26del
NM_152287.4:c.*756_*760del (ZNF276)	NP_689500.2:n.*756_*760del
NR_110122.2:n.2756_2760del (ZNF276)
NR_110126.2:n.2639_2643del (ZNF276)
NR_110129.2:n.2673_2677del (ZNF276)
NR_110128.2:n.2579_2583del (ZNF276)