Canonical Allele Identifier: CA397484314

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805572G>C (hg19) ; chr16:g.89739164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739164G>C , CM000678.2:g.89739164G>C	GRCh38
NC_000016.9:g.89805572G>C , CM000678.1:g.89805572G>C	GRCh37
NC_000016.8:g.88333073G>C	NCBI36
NG_011706.1:g.82494C>G , LRG_495:g.82494C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2709C>G (FANCA)	ENSP00000512522.1:n.*2709C>G
ENST00000564475.6:c.4136C>G (FANCA)	ENSP00000454977.2:p.Pro1379Arg
ENST00000567510.2:c.2706C>G (FANCA)	ENSP00000455969.1:n.2706C>G
ENST00000568369.6:c.4136C>G (FANCA)	ENSP00000456829.1:p.Pro1379Arg
ENST00000696274.1:n.4097C>G (FANCA)
ENST00000696275.1:c.*3371C>G (FANCA)	ENSP00000512517.1:n.*3371C>G
ENST00000696286.1:c.*49C>G (FANCA)	ENSP00000512523.1:n.*49C>G
ENST00000696287.1:c.4007C>G (FANCA)	ENSP00000512524.1:p.Pro1336Arg
ENST00000696291.1:c.*3568C>G (FANCA)	ENSP00000512530.1:n.*3568C>G
ENST00000389301.8:c.4136C>G (FANCA) MANE Select	ENSP00000373952.3:p.Pro1379Arg
ENST00000443381.7:c.*918G>C (ZNF276) MANE Select	ENSP00000415836.2:n.*918G>C
ENST00000289816.9:c.*918G>C (ZNF276)	ENSP00000289816.5:n.*918G>C
ENST00000389301.7:c.4136C>G (FANCA)	ENSP00000373952.3:p.Pro1379Arg
ENST00000561722.5:c.287C>G (FANCA)	ENSP00000456608.1:p.Pro96Arg
ENST00000562424.1:n.407C>G (FANCA)
ENST00000563983.5:n.2751G>C (ZNF276)
ENST00000564475.5:c.466C>G (FANCA)
ENST00000564870.1:c.337C>G (FANCA)
ENST00000567879.5:c.515C>G (FANCA)	ENSP00000457006.1:p.Pro172Arg
ENST00000568369.5:c.4136C>G (FANCA)	ENSP00000456829.1:p.Pro1379Arg
NM_000135.2:c.4136C>G , LRG_495t1:c.4136C>G (FANCA)	NP_000126.2:p.Pro1379Arg
NM_001113525.1:c.*918G>C (ZNF276)	NP_001106997.1:n.*918G>C
NM_001286167.1:c.4136C>G (FANCA)	NP_001273096.1:p.Pro1379Arg
NM_152287.3:c.*918G>C (ZNF276)	NP_689500.2:n.*918G>C
NR_110122.1:n.2935G>C (ZNF276)
NR_110126.1:n.2818G>C (ZNF276)
NR_110128.1:n.2741G>C (ZNF276)
NR_110129.1:n.2830G>C (ZNF276)
XM_005256294.3:c.4136C>G (FANCA)	XP_005256351.1:p.Pro1379Arg
XM_011522945.1:c.4007C>G (FANCA)	XP_011521247.1:p.Pro1336Arg
XM_011522946.1:c.3113C>G (FANCA)	XP_011521248.1:p.Pro1038Arg
XM_011522947.1:c.3113C>G (FANCA)	XP_011521249.1:p.Pro1038Arg
XR_933244.1:n.4103C>G (FANCA)
XR_933245.1:n.4040C>G (FANCA)
NM_000135.3:c.4136C>G (FANCA)	NP_000126.2:p.Pro1379Arg
NM_001286167.2:c.4136C>G (FANCA)	NP_001273096.1:p.Pro1379Arg
XM_005256294.4:c.4136C>G (FANCA)	XP_005256351.1:p.Pro1379Arg
XM_011522945.2:c.4007C>G (FANCA)	XP_011521247.1:p.Pro1336Arg
XM_011522946.3:c.3113C>G (FANCA)	XP_011521248.1:p.Pro1038Arg
XM_011522947.2:c.3113C>G (FANCA)	XP_011521249.1:p.Pro1038Arg
XM_017023044.2:c.4007C>G (FANCA)	XP_016878533.1:p.Pro1336Arg
XM_017023890.1:c.*918G>C (ZNF276)	XP_016879379.1:n.*918G>C
XM_024450189.1:c.3113C>G (FANCA)	XP_024305957.1:p.Pro1038Arg
XR_933244.2:n.4103C>G (FANCA)
XR_933245.2:n.4040C>G (FANCA)
XR_933484.2:n.2929G>C (ZNF276)
NM_000135.4:c.4136C>G (FANCA) MANE Select	NP_000126.2:p.Pro1379Arg
NM_001113525.2:c.*918G>C (ZNF276) MANE Select	NP_001106997.1:n.*918G>C
NM_001286167.3:c.4136C>G (FANCA)	NP_001273096.1:p.Pro1379Arg
NM_152287.4:c.*918G>C (ZNF276)	NP_689500.2:n.*918G>C
NR_110122.2:n.2918G>C (ZNF276)
NR_110126.2:n.2801G>C (ZNF276)
NR_110129.2:n.2835G>C (ZNF276)
NR_110128.2:n.2741G>C (ZNF276)