Canonical Allele Identifier: CA397483529

Gene: FANCA ZNF276

Linked Data

• dbSNP Id: rs1255828474
• gnomAD v2: 16-89805344-A-C
• gnomAD v3: 16-89738936-A-C
• gnomAD v4: 16-89738936-A-C
• MyVariant Identifiers: chr16:g.89805344A>C (hg19) ; chr16:g.89738936A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738936A>C , CM000678.2:g.89738936A>C	GRCh38
NC_000016.9:g.89805344A>C , CM000678.1:g.89805344A>C	GRCh37
NC_000016.8:g.88332845A>C	NCBI36
NG_011706.1:g.82722T>G , LRG_495:g.82722T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2779T>G (FANCA)	ENSP00000512522.1:n.*2779T>G
ENST00000564475.6:c.4210T>G (FANCA)	ENSP00000454977.2:p.Ser1404Ala
ENST00000567510.2:c.2780T>G (FANCA)	ENSP00000455969.1:n.2780T>G
ENST00000568369.6:c.4210T>G (FANCA)	ENSP00000456829.1:p.Ser1404Ala
ENST00000696274.1:n.4167T>G (FANCA)
ENST00000696275.1:c.*3445T>G (FANCA)	ENSP00000512517.1:n.*3445T>G
ENST00000696286.1:c.*119T>G (FANCA)	ENSP00000512523.1:n.*119T>G
ENST00000696287.1:c.4081T>G (FANCA)	ENSP00000512524.1:p.Ser1361Ala
ENST00000696291.1:c.*3638T>G (FANCA)	ENSP00000512530.1:n.*3638T>G
ENST00000389301.8:c.4206T>G (FANCA) MANE Select	ENSP00000373952.3:p.Phe1402Leu
ENST00000443381.7:c.*690A>C (ZNF276) MANE Select	ENSP00000415836.2:n.*690A>C
ENST00000289816.9:c.*690A>C (ZNF276)	ENSP00000289816.5:n.*690A>C
ENST00000389301.7:c.4206T>G (FANCA)	ENSP00000373952.3:p.Phe1402Leu
ENST00000561722.5:c.436-10T>G (FANCA)	ENSP00000456608.1:n.436-10T>G
ENST00000562424.1:n.477T>G (FANCA)
ENST00000563983.5:n.2523A>C (ZNF276)
ENST00000564475.5:c.540T>G (FANCA)
ENST00000564870.1:c.407T>G (FANCA)
ENST00000567879.5:c.580T>G (FANCA)	ENSP00000457006.1:p.Ser194Ala
ENST00000568369.5:c.4210T>G (FANCA)	ENSP00000456829.1:p.Ser1404Ala
NM_000135.2:c.4206T>G , LRG_495t1:c.4206T>G (FANCA)	NP_000126.2:p.Phe1402Leu
NM_001113525.1:c.*690A>C (ZNF276)	NP_001106997.1:n.*690A>C
NM_001286167.1:c.4210T>G (FANCA)	NP_001273096.1:p.Ser1404Ala
NM_152287.3:c.*690A>C (ZNF276)	NP_689500.2:n.*690A>C
NR_110122.1:n.2707A>C (ZNF276)
NR_110126.1:n.2590A>C (ZNF276)
NR_110128.1:n.2513A>C (ZNF276)
NR_110129.1:n.2602A>C (ZNF276)
XM_005256294.3:c.4210T>G (FANCA)	XP_005256351.1:p.Ser1404Ala
XM_011522945.1:c.4081T>G (FANCA)	XP_011521247.1:p.Ser1361Ala
XM_011522946.1:c.3187T>G (FANCA)	XP_011521248.1:p.Ser1063Ala
XM_011522947.1:c.3187T>G (FANCA)	XP_011521249.1:p.Ser1063Ala
XR_933244.1:n.4173T>G (FANCA)
XR_933245.1:n.4110T>G (FANCA)
NM_000135.3:c.4206T>G (FANCA)	NP_000126.2:p.Phe1402Leu
NM_001286167.2:c.4210T>G (FANCA)	NP_001273096.1:p.Ser1404Ala
XM_005256294.4:c.4210T>G (FANCA)	XP_005256351.1:p.Ser1404Ala
XM_011522945.2:c.4081T>G (FANCA)	XP_011521247.1:p.Ser1361Ala
XM_011522946.3:c.3187T>G (FANCA)	XP_011521248.1:p.Ser1063Ala
XM_011522947.2:c.3187T>G (FANCA)	XP_011521249.1:p.Ser1063Ala
XM_017023044.2:c.4077T>G (FANCA)	XP_016878533.1:p.Phe1359Leu
XM_017023890.1:c.*690A>C (ZNF276)	XP_016879379.1:n.*690A>C
XM_024450189.1:c.3187T>G (FANCA)	XP_024305957.1:p.Ser1063Ala
XR_933244.2:n.4173T>G (FANCA)
XR_933245.2:n.4110T>G (FANCA)
XR_933484.2:n.2701A>C (ZNF276)
NM_000135.4:c.4206T>G (FANCA) MANE Select	NP_000126.2:p.Phe1402Leu
NM_001113525.2:c.*690A>C (ZNF276) MANE Select	NP_001106997.1:n.*690A>C
NM_001286167.3:c.4210T>G (FANCA)	NP_001273096.1:p.Ser1404Ala
NM_152287.4:c.*690A>C (ZNF276)	NP_689500.2:n.*690A>C
NR_110122.2:n.2690A>C (ZNF276)
NR_110126.2:n.2573A>C (ZNF276)
NR_110129.2:n.2607A>C (ZNF276)
NR_110128.2:n.2513A>C (ZNF276)