Canonical Allele Identifier: CA397484295

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805561T>G (hg19) ; chr16:g.89739153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739153T>G , CM000678.2:g.89739153T>G	GRCh38
NC_000016.9:g.89805561T>G , CM000678.1:g.89805561T>G	GRCh37
NC_000016.8:g.88333062T>G	NCBI36
NG_011706.1:g.82505A>C , LRG_495:g.82505A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2720A>C (FANCA)	ENSP00000512522.1:n.*2720A>C
ENST00000564475.6:c.4147A>C (FANCA)	ENSP00000454977.2:p.Ser1383Arg
ENST00000567510.2:c.2717A>C (FANCA)	ENSP00000455969.1:n.2717A>C
ENST00000568369.6:c.4147A>C (FANCA)	ENSP00000456829.1:p.Ser1383Arg
ENST00000696274.1:n.4108A>C (FANCA)
ENST00000696275.1:c.*3382A>C (FANCA)	ENSP00000512517.1:n.*3382A>C
ENST00000696286.1:c.*60A>C (FANCA)	ENSP00000512523.1:n.*60A>C
ENST00000696287.1:c.4018A>C (FANCA)	ENSP00000512524.1:p.Ser1340Arg
ENST00000696291.1:c.*3579A>C (FANCA)	ENSP00000512530.1:n.*3579A>C
ENST00000389301.8:c.4147A>C (FANCA) MANE Select	ENSP00000373952.3:p.Ser1383Arg
ENST00000443381.7:c.*907T>G (ZNF276) MANE Select	ENSP00000415836.2:n.*907T>G
ENST00000289816.9:c.*907T>G (ZNF276)	ENSP00000289816.5:n.*907T>G
ENST00000389301.7:c.4147A>C (FANCA)	ENSP00000373952.3:p.Ser1383Arg
ENST00000561722.5:c.298A>C (FANCA)	ENSP00000456608.1:p.Ser100Arg
ENST00000562424.1:n.418A>C (FANCA)
ENST00000563983.5:n.2740T>G (ZNF276)
ENST00000564475.5:c.477A>C (FANCA)
ENST00000564870.1:c.348A>C (FANCA)
ENST00000567879.5:c.526A>C (FANCA)	ENSP00000457006.1:p.Ser176Arg
ENST00000568369.5:c.4147A>C (FANCA)	ENSP00000456829.1:p.Ser1383Arg
NM_000135.2:c.4147A>C , LRG_495t1:c.4147A>C (FANCA)	NP_000126.2:p.Ser1383Arg
NM_001113525.1:c.*907T>G (ZNF276)	NP_001106997.1:n.*907T>G
NM_001286167.1:c.4147A>C (FANCA)	NP_001273096.1:p.Ser1383Arg
NM_152287.3:c.*907T>G (ZNF276)	NP_689500.2:n.*907T>G
NR_110122.1:n.2924T>G (ZNF276)
NR_110126.1:n.2807T>G (ZNF276)
NR_110128.1:n.2730T>G (ZNF276)
NR_110129.1:n.2819T>G (ZNF276)
XM_005256294.3:c.4147A>C (FANCA)	XP_005256351.1:p.Ser1383Arg
XM_011522945.1:c.4018A>C (FANCA)	XP_011521247.1:p.Ser1340Arg
XM_011522946.1:c.3124A>C (FANCA)	XP_011521248.1:p.Ser1042Arg
XM_011522947.1:c.3124A>C (FANCA)	XP_011521249.1:p.Ser1042Arg
XR_933244.1:n.4114A>C (FANCA)
XR_933245.1:n.4051A>C (FANCA)
NM_000135.3:c.4147A>C (FANCA)	NP_000126.2:p.Ser1383Arg
NM_001286167.2:c.4147A>C (FANCA)	NP_001273096.1:p.Ser1383Arg
XM_005256294.4:c.4147A>C (FANCA)	XP_005256351.1:p.Ser1383Arg
XM_011522945.2:c.4018A>C (FANCA)	XP_011521247.1:p.Ser1340Arg
XM_011522946.3:c.3124A>C (FANCA)	XP_011521248.1:p.Ser1042Arg
XM_011522947.2:c.3124A>C (FANCA)	XP_011521249.1:p.Ser1042Arg
XM_017023044.2:c.4018A>C (FANCA)	XP_016878533.1:p.Ser1340Arg
XM_017023890.1:c.*907T>G (ZNF276)	XP_016879379.1:n.*907T>G
XM_024450189.1:c.3124A>C (FANCA)	XP_024305957.1:p.Ser1042Arg
XR_933244.2:n.4114A>C (FANCA)
XR_933245.2:n.4051A>C (FANCA)
XR_933484.2:n.2918T>G (ZNF276)
NM_000135.4:c.4147A>C (FANCA) MANE Select	NP_000126.2:p.Ser1383Arg
NM_001113525.2:c.*907T>G (ZNF276) MANE Select	NP_001106997.1:n.*907T>G
NM_001286167.3:c.4147A>C (FANCA)	NP_001273096.1:p.Ser1383Arg
NM_152287.4:c.*907T>G (ZNF276)	NP_689500.2:n.*907T>G
NR_110122.2:n.2907T>G (ZNF276)
NR_110126.2:n.2790T>G (ZNF276)
NR_110129.2:n.2824T>G (ZNF276)
NR_110128.2:n.2730T>G (ZNF276)