Canonical Allele Identifier: CA2635025026

Gene: FANCA ZNF276

Linked Data

• gnomAD v4: 16-89739520-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739522del , CM000678.2:g.89739522del	GRCh38
NC_000016.9:g.89805930del , CM000678.1:g.89805930del	GRCh37
NC_000016.8:g.88333431del	NCBI36
NG_011706.1:g.82137del , LRG_495:g.82137del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561667.2:c.*2540del (FANCA)	ENSP00000512522.1:n.*2540del
ENST00000564475.6:c.3967del (FANCA)	ENSP00000454977.2:p.Ala1323ProfsTer?
ENST00000567510.2:c.2537del (FANCA)	ENSP00000455969.1:n.2537del
ENST00000568369.6:c.3967del (FANCA)	ENSP00000456829.1:p.Ala1323ProfsTer?
ENST00000696274.1:n.3928del (FANCA)
ENST00000696275.1:c.*3202del (FANCA)	ENSP00000512517.1:n.*3202del
ENST00000696286.1:c.3935-232del (FANCA)	ENSP00000512523.1:n.3935-232del
ENST00000696287.1:c.3838del (FANCA)	ENSP00000512524.1:p.Ala1280ProfsTer?
ENST00000696291.1:c.*3399del (FANCA)	ENSP00000512530.1:n.*3399del
ENST00000389301.8:c.3967del (FANCA) MANE Select	ENSP00000373952.3:p.Ala1323ProfsTer?
ENST00000443381.7:c.*1276del (ZNF276) MANE Select	ENSP00000415836.2:n.*1276del
ENST00000289816.9:c.*1276del (ZNF276)	ENSP00000289816.5:n.*1276del
ENST00000389301.7:c.3967del (FANCA)	ENSP00000373952.3:p.Ala1323ProfsTer?
ENST00000561722.5:c.118del (FANCA)	ENSP00000456608.1:p.Ala40ProfsTer?
ENST00000562424.1:n.238del (FANCA)
ENST00000563983.5:n.3109del (ZNF276)
ENST00000564475.5:c.297del (FANCA)
ENST00000564870.1:c.168del (FANCA)
ENST00000564969.5:n.692del (FANCA)
ENST00000567879.5:c.413-255del (FANCA)	ENSP00000457006.1:n.413-255del
ENST00000568369.5:c.3967del (FANCA)	ENSP00000456829.1:p.Ala1323ProfsTer?
ENST00000568626.1:c.676del (FANCA)
NM_000135.2:c.3967del , LRG_495t1:c.3967del (FANCA)	NP_000126.2:p.Ala1323ProfsTer?
NM_001113525.1:c.*1276del (ZNF276)	NP_001106997.1:n.*1276del
NM_001286167.1:c.3967del (FANCA)	NP_001273096.1:p.Ala1323ProfsTer?
NM_152287.3:c.*1276del (ZNF276)	NP_689500.2:n.*1276del
NR_110122.1:n.3293del (ZNF276)
NR_110126.1:n.3176del (ZNF276)
NR_110128.1:n.3099del (ZNF276)
NR_110129.1:n.3188del (ZNF276)
XM_005256294.3:c.3967del (FANCA)	XP_005256351.1:p.Ala1323ProfsTer?
XM_011522945.1:c.3838del (FANCA)	XP_011521247.1:p.Ala1280ProfsTer?
XM_011522946.1:c.2944del (FANCA)	XP_011521248.1:p.Ala982ProfsTer?
XM_011522947.1:c.2944del (FANCA)	XP_011521249.1:p.Ala982ProfsTer?
XR_933244.1:n.3978-232del (FANCA)
XR_933245.1:n.3871del (FANCA)
NM_000135.3:c.3967del (FANCA)	NP_000126.2:p.Ala1323ProfsTer?
NM_001286167.2:c.3967del (FANCA)	NP_001273096.1:p.Ala1323ProfsTer?
XM_005256294.4:c.3967del (FANCA)	XP_005256351.1:p.Ala1323ProfsTer?
XM_011522945.2:c.3838del (FANCA)	XP_011521247.1:p.Ala1280ProfsTer?
XM_011522946.3:c.2944del (FANCA)	XP_011521248.1:p.Ala982ProfsTer?
XM_011522947.2:c.2944del (FANCA)	XP_011521249.1:p.Ala982ProfsTer?
XM_017023044.2:c.3838del (FANCA)	XP_016878533.1:p.Ala1280ProfsTer?
XM_017023890.1:c.*1276del (ZNF276)	XP_016879379.1:n.*1276del
XM_024450189.1:c.2944del (FANCA)	XP_024305957.1:p.Ala982ProfsTer?
XR_001751866.1:n.3837del (FANCA)
XR_933244.2:n.3978-232del (FANCA)
XR_933245.2:n.3871del (FANCA)
XR_933484.2:n.3287del (ZNF276)
NM_000135.4:c.3967del (FANCA) MANE Select	NP_000126.2:p.Ala1323ProfsTer?
NM_001113525.2:c.*1276del (ZNF276) MANE Select	NP_001106997.1:n.*1276del
NM_001286167.3:c.3967del (FANCA)	NP_001273096.1:p.Ala1323ProfsTer?
NM_152287.4:c.*1276del (ZNF276)	NP_689500.2:n.*1276del
NR_110122.2:n.3276del (ZNF276)
NR_110126.2:n.3159del (ZNF276)
NR_110129.2:n.3193del (ZNF276)
NR_110128.2:n.3099del (ZNF276)