Canonical Allele Identifier: CA2576101711

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89738982-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738985_89738986del , CM000678.2:g.89738985_89738986del	GRCh38
NC_000016.9:g.89805393_89805394del , CM000678.1:g.89805393_89805394del	GRCh37
NC_000016.8:g.88332894_88332895del	NCBI36
NG_011706.1:g.82674_82675del , LRG_495:g.82674_82675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2741-10_*2741-9del (FANCA)	ENSP00000512522.1:n.*2741-10_*2741-9del
ENST00000564475.6:c.4172-10_4172-9del (FANCA)	ENSP00000454977.2:n.4172-10_4172-9del
ENST00000567510.2:c.2742-10_2742-9del (FANCA)	ENSP00000455969.1:n.2742-10_2742-9del
ENST00000568369.6:c.4172-10_4172-9del (FANCA)	ENSP00000456829.1:n.4172-10_4172-9del
ENST00000696274.1:n.4129-10_4129-9del (FANCA)
ENST00000696275.1:c.*3407-10_*3407-9del (FANCA)	ENSP00000512517.1:n.*3407-10_*3407-9del
ENST00000696286.1:c.*81-10_*81-9del (FANCA)	ENSP00000512523.1:n.*81-10_*81-9del
ENST00000696287.1:c.4043-10_4043-9del (FANCA)	ENSP00000512524.1:n.4043-10_4043-9del
ENST00000696291.1:c.*3600-10_*3600-9del (FANCA)	ENSP00000512530.1:n.*3600-10_*3600-9del
ENST00000389301.8:c.4168-10_4168-9del (FANCA) MANE Select	ENSP00000373952.3:n.4168-10_4168-9del
ENST00000443381.7:c.*739_*740del (ZNF276) MANE Select	ENSP00000415836.2:n.*739_*740del
ENST00000289816.9:c.*739_*740del (ZNF276)	ENSP00000289816.5:n.*739_*740del
ENST00000389301.7:c.4168-10_4168-9del (FANCA)	ENSP00000373952.3:n.4168-10_4168-9del
ENST00000561722.5:c.435+32_435+33del (FANCA)	ENSP00000456608.1:n.435+32_435+33del
ENST00000562424.1:n.439-10_439-9del (FANCA)
ENST00000563983.5:n.2572_2573del (ZNF276)
ENST00000564475.5:c.502-10_502-9del (FANCA)
ENST00000564870.1:c.369-10_369-9del (FANCA)
ENST00000567879.5:c.542-10_542-9del (FANCA)	ENSP00000457006.1:n.542-10_542-9del
ENST00000568369.5:c.4172-10_4172-9del (FANCA)	ENSP00000456829.1:n.4172-10_4172-9del
NM_000135.2:c.4168-10_4168-9del , LRG_495t1:c.4168-10_4168-9del (FANCA)	NP_000126.2:n.4168-10_4168-9del
NM_001113525.1:c.*739_*740del (ZNF276)	NP_001106997.1:n.*739_*740del
NM_001286167.1:c.4172-10_4172-9del (FANCA)	NP_001273096.1:n.4172-10_4172-9del
NM_152287.3:c.*739_*740del (ZNF276)	NP_689500.2:n.*739_*740del
NR_110122.1:n.2756_2757del (ZNF276)
NR_110126.1:n.2639_2640del (ZNF276)
NR_110128.1:n.2562_2563del (ZNF276)
NR_110129.1:n.2651_2652del (ZNF276)
XM_005256294.3:c.4172-10_4172-9del (FANCA)	XP_005256351.1:n.4172-10_4172-9del
XM_011522945.1:c.4043-10_4043-9del (FANCA)	XP_011521247.1:n.4043-10_4043-9del
XM_011522946.1:c.3149-10_3149-9del (FANCA)	XP_011521248.1:n.3149-10_3149-9del
XM_011522947.1:c.3149-10_3149-9del (FANCA)	XP_011521249.1:n.3149-10_3149-9del
XR_933244.1:n.4135-10_4135-9del (FANCA)
XR_933245.1:n.4072-10_4072-9del (FANCA)
NM_000135.3:c.4168-10_4168-9del (FANCA)	NP_000126.2:n.4168-10_4168-9del
NM_001286167.2:c.4172-10_4172-9del (FANCA)	NP_001273096.1:n.4172-10_4172-9del
XM_005256294.4:c.4172-10_4172-9del (FANCA)	XP_005256351.1:n.4172-10_4172-9del
XM_011522945.2:c.4043-10_4043-9del (FANCA)	XP_011521247.1:n.4043-10_4043-9del
XM_011522946.3:c.3149-10_3149-9del (FANCA)	XP_011521248.1:n.3149-10_3149-9del
XM_011522947.2:c.3149-10_3149-9del (FANCA)	XP_011521249.1:n.3149-10_3149-9del
XM_017023044.2:c.4039-10_4039-9del (FANCA)	XP_016878533.1:n.4039-10_4039-9del
XM_017023890.1:c.*739_*740del (ZNF276)	XP_016879379.1:n.*739_*740del
XM_024450189.1:c.3149-10_3149-9del (FANCA)	XP_024305957.1:n.3149-10_3149-9del
XR_933244.2:n.4135-10_4135-9del (FANCA)
XR_933245.2:n.4072-10_4072-9del (FANCA)
XR_933484.2:n.2750_2751del (ZNF276)
NM_000135.4:c.4168-10_4168-9del (FANCA) MANE Select	NP_000126.2:n.4168-10_4168-9del
NM_001113525.2:c.*739_*740del (ZNF276) MANE Select	NP_001106997.1:n.*739_*740del
NM_001286167.3:c.4172-10_4172-9del (FANCA)	NP_001273096.1:n.4172-10_4172-9del
NM_152287.4:c.*739_*740del (ZNF276)	NP_689500.2:n.*739_*740del
NR_110122.2:n.2739_2740del (ZNF276)
NR_110126.2:n.2622_2623del (ZNF276)
NR_110129.2:n.2656_2657del (ZNF276)
NR_110128.2:n.2562_2563del (ZNF276)