Canonical Allele Identifier: CA8250689

Gene: FANCA ZNF276

Linked Data

• dbSNP Id: rs754170870
• ExAC: 16:89805343 G / GA
• gnomAD v2: 16-89805343-G-GA
• gnomAD v4: 16-89738935-G-GA
• MyVariant Identifiers: chr16:g.89805343_89805344insA (hg19) ; chr16:g.89738935_89738936insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738940dup , CM000678.2:g.89738940dup	GRCh38
NC_000016.9:g.89805348dup , CM000678.1:g.89805348dup	GRCh37
NC_000016.8:g.88332849dup	NCBI36
NG_011706.1:g.82722dup , LRG_495:g.82722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2779dup (FANCA)	ENSP00000512522.1:n.*2779dup
ENST00000564475.6:c.4210dup (FANCA)	ENSP00000454977.2:p.Ser1404PhefsTer5
ENST00000567510.2:c.2780dup (FANCA)	ENSP00000455969.1:n.2780dup
ENST00000568369.6:c.4210dup (FANCA)	ENSP00000456829.1:p.Ser1404PhefsTer5
ENST00000696274.1:n.4167dup (FANCA)
ENST00000696275.1:c.*3445dup (FANCA)	ENSP00000512517.1:n.*3445dup
ENST00000696286.1:c.*119dup (FANCA)	ENSP00000512523.1:n.*119dup
ENST00000696287.1:c.4081dup (FANCA)	ENSP00000512524.1:p.Ser1361PhefsTer5
ENST00000696291.1:c.*3638dup (FANCA)	ENSP00000512530.1:n.*3638dup
ENST00000389301.8:c.4206dup (FANCA) MANE Select	ENSP00000373952.3:p.Leu1403SerfsTer22
ENST00000443381.7:c.*694dup (ZNF276) MANE Select	ENSP00000415836.2:n.*694dup
ENST00000289816.9:c.*694dup (ZNF276)	ENSP00000289816.5:n.*694dup
ENST00000389301.7:c.4206dup (FANCA)	ENSP00000373952.3:p.Leu1403SerfsTer22
ENST00000561722.5:c.436-10dup (FANCA)	ENSP00000456608.1:n.436-10dup
ENST00000562424.1:n.477dup (FANCA)
ENST00000563983.5:n.2527dup (ZNF276)
ENST00000564475.5:c.540dup (FANCA)
ENST00000564870.1:c.407dup (FANCA)
ENST00000567879.5:c.580dup (FANCA)	ENSP00000457006.1:p.Ser194PhefsTer5
ENST00000568369.5:c.4210dup (FANCA)	ENSP00000456829.1:p.Ser1404PhefsTer5
NM_000135.2:c.4206dup , LRG_495t1:c.4206dup (FANCA)	NP_000126.2:p.Leu1403SerfsTer22
NM_001113525.1:c.*694dup (ZNF276)	NP_001106997.1:n.*694dup
NM_001286167.1:c.4210dup (FANCA)	NP_001273096.1:p.Ser1404PhefsTer5
NM_152287.3:c.*694dup (ZNF276)	NP_689500.2:n.*694dup
NR_110122.1:n.2711dup (ZNF276)
NR_110126.1:n.2594dup (ZNF276)
NR_110128.1:n.2517dup (ZNF276)
NR_110129.1:n.2606dup (ZNF276)
XM_005256294.3:c.4210dup (FANCA)	XP_005256351.1:p.Ser1404PhefsTer5
XM_011522945.1:c.4081dup (FANCA)	XP_011521247.1:p.Ser1361PhefsTer5
XM_011522946.1:c.3187dup (FANCA)	XP_011521248.1:p.Ser1063PhefsTer5
XM_011522947.1:c.3187dup (FANCA)	XP_011521249.1:p.Ser1063PhefsTer5
XR_933244.1:n.4173dup (FANCA)
XR_933245.1:n.4110dup (FANCA)
NM_000135.3:c.4206dup (FANCA)	NP_000126.2:p.Leu1403SerfsTer22
NM_001286167.2:c.4210dup (FANCA)	NP_001273096.1:p.Ser1404PhefsTer5
XM_005256294.4:c.4210dup (FANCA)	XP_005256351.1:p.Ser1404PhefsTer5
XM_011522945.2:c.4081dup (FANCA)	XP_011521247.1:p.Ser1361PhefsTer5
XM_011522946.3:c.3187dup (FANCA)	XP_011521248.1:p.Ser1063PhefsTer5
XM_011522947.2:c.3187dup (FANCA)	XP_011521249.1:p.Ser1063PhefsTer5
XM_017023044.2:c.4077dup (FANCA)	XP_016878533.1:p.Leu1360SerfsTer22
XM_017023890.1:c.*694dup (ZNF276)	XP_016879379.1:n.*694dup
XM_024450189.1:c.3187dup (FANCA)	XP_024305957.1:p.Ser1063PhefsTer5
XR_933244.2:n.4173dup (FANCA)
XR_933245.2:n.4110dup (FANCA)
XR_933484.2:n.2705dup (ZNF276)
NM_000135.4:c.4206dup (FANCA) MANE Select	NP_000126.2:p.Leu1403SerfsTer22
NM_001113525.2:c.*694dup (ZNF276) MANE Select	NP_001106997.1:n.*694dup
NM_001286167.3:c.4210dup (FANCA)	NP_001273096.1:p.Ser1404PhefsTer5
NM_152287.4:c.*694dup (ZNF276)	NP_689500.2:n.*694dup
NR_110122.2:n.2694dup (ZNF276)
NR_110126.2:n.2577dup (ZNF276)
NR_110129.2:n.2611dup (ZNF276)
NR_110128.2:n.2517dup (ZNF276)