Canonical Allele Identifier: CA397483597

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805353A>G (hg19) ; chr16:g.89738945A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738945A>G , CM000678.2:g.89738945A>G	GRCh38
NC_000016.9:g.89805353A>G , CM000678.1:g.89805353A>G	GRCh37
NC_000016.8:g.88332854A>G	NCBI36
NG_011706.1:g.82713T>C , LRG_495:g.82713T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2770T>C (FANCA)	ENSP00000512522.1:n.*2770T>C
ENST00000564475.6:c.4201T>C (FANCA)	ENSP00000454977.2:p.Ser1401Pro
ENST00000567510.2:c.2771T>C (FANCA)	ENSP00000455969.1:n.2771T>C
ENST00000568369.6:c.4201T>C (FANCA)	ENSP00000456829.1:p.Ser1401Pro
ENST00000696274.1:n.4158T>C (FANCA)
ENST00000696275.1:c.*3436T>C (FANCA)	ENSP00000512517.1:n.*3436T>C
ENST00000696286.1:c.*110T>C (FANCA)	ENSP00000512523.1:n.*110T>C
ENST00000696287.1:c.4072T>C (FANCA)	ENSP00000512524.1:p.Ser1358Pro
ENST00000696291.1:c.*3629T>C (FANCA)	ENSP00000512530.1:n.*3629T>C
ENST00000389301.8:c.4197T>C (FANCA) MANE Select	ENSP00000373952.3:p.Ala1399=
ENST00000443381.7:c.*699A>G (ZNF276) MANE Select	ENSP00000415836.2:n.*699A>G
ENST00000289816.9:c.*699A>G (ZNF276)	ENSP00000289816.5:n.*699A>G
ENST00000389301.7:c.4197T>C (FANCA)	ENSP00000373952.3:p.Ala1399=
ENST00000561722.5:c.436-19T>C (FANCA)	ENSP00000456608.1:n.436-19T>C
ENST00000562424.1:n.468T>C (FANCA)
ENST00000563983.5:n.2532A>G (ZNF276)
ENST00000564475.5:c.531T>C (FANCA)
ENST00000564870.1:c.398T>C (FANCA)
ENST00000567879.5:c.571T>C (FANCA)	ENSP00000457006.1:p.Ser191Pro
ENST00000568369.5:c.4201T>C (FANCA)	ENSP00000456829.1:p.Ser1401Pro
NM_000135.2:c.4197T>C , LRG_495t1:c.4197T>C (FANCA)	NP_000126.2:p.Ala1399=
NM_001113525.1:c.*699A>G (ZNF276)	NP_001106997.1:n.*699A>G
NM_001286167.1:c.4201T>C (FANCA)	NP_001273096.1:p.Ser1401Pro
NM_152287.3:c.*699A>G (ZNF276)	NP_689500.2:n.*699A>G
NR_110122.1:n.2716A>G (ZNF276)
NR_110126.1:n.2599A>G (ZNF276)
NR_110128.1:n.2522A>G (ZNF276)
NR_110129.1:n.2611A>G (ZNF276)
XM_005256294.3:c.4201T>C (FANCA)	XP_005256351.1:p.Ser1401Pro
XM_011522945.1:c.4072T>C (FANCA)	XP_011521247.1:p.Ser1358Pro
XM_011522946.1:c.3178T>C (FANCA)	XP_011521248.1:p.Ser1060Pro
XM_011522947.1:c.3178T>C (FANCA)	XP_011521249.1:p.Ser1060Pro
XR_933244.1:n.4164T>C (FANCA)
XR_933245.1:n.4101T>C (FANCA)
NM_000135.3:c.4197T>C (FANCA)	NP_000126.2:p.Ala1399=
NM_001286167.2:c.4201T>C (FANCA)	NP_001273096.1:p.Ser1401Pro
XM_005256294.4:c.4201T>C (FANCA)	XP_005256351.1:p.Ser1401Pro
XM_011522945.2:c.4072T>C (FANCA)	XP_011521247.1:p.Ser1358Pro
XM_011522946.3:c.3178T>C (FANCA)	XP_011521248.1:p.Ser1060Pro
XM_011522947.2:c.3178T>C (FANCA)	XP_011521249.1:p.Ser1060Pro
XM_017023044.2:c.4068T>C (FANCA)	XP_016878533.1:p.Ala1356=
XM_017023890.1:c.*699A>G (ZNF276)	XP_016879379.1:n.*699A>G
XM_024450189.1:c.3178T>C (FANCA)	XP_024305957.1:p.Ser1060Pro
XR_933244.2:n.4164T>C (FANCA)
XR_933245.2:n.4101T>C (FANCA)
XR_933484.2:n.2710A>G (ZNF276)
NM_000135.4:c.4197T>C (FANCA) MANE Select	NP_000126.2:p.Ala1399=
NM_001113525.2:c.*699A>G (ZNF276) MANE Select	NP_001106997.1:n.*699A>G
NM_001286167.3:c.4201T>C (FANCA)	NP_001273096.1:p.Ser1401Pro
NM_152287.4:c.*699A>G (ZNF276)	NP_689500.2:n.*699A>G
NR_110122.2:n.2699A>G (ZNF276)
NR_110126.2:n.2582A>G (ZNF276)
NR_110129.2:n.2616A>G (ZNF276)
NR_110128.2:n.2522A>G (ZNF276)