Canonical Allele Identifier: CA397484818

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805928G>C (hg19) ; chr16:g.89739520G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739520G>C , CM000678.2:g.89739520G>C	GRCh38
NC_000016.9:g.89805928G>C , CM000678.1:g.89805928G>C	GRCh37
NC_000016.8:g.88333429G>C	NCBI36
NG_011706.1:g.82138C>G , LRG_495:g.82138C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561667.2:c.*2541C>G (FANCA)	ENSP00000512522.1:n.*2541C>G
ENST00000564475.6:c.3968C>G (FANCA)	ENSP00000454977.2:p.Ala1323Gly
ENST00000567510.2:c.2538C>G (FANCA)	ENSP00000455969.1:n.2538C>G
ENST00000568369.6:c.3968C>G (FANCA)	ENSP00000456829.1:p.Ala1323Gly
ENST00000696274.1:n.3929C>G (FANCA)
ENST00000696275.1:c.*3203C>G (FANCA)	ENSP00000512517.1:n.*3203C>G
ENST00000696286.1:c.3935-231C>G (FANCA)	ENSP00000512523.1:n.3935-231C>G
ENST00000696287.1:c.3839C>G (FANCA)	ENSP00000512524.1:p.Ala1280Gly
ENST00000696291.1:c.*3400C>G (FANCA)	ENSP00000512530.1:n.*3400C>G
ENST00000389301.8:c.3968C>G (FANCA) MANE Select	ENSP00000373952.3:p.Ala1323Gly
ENST00000443381.7:c.*1274G>C (ZNF276) MANE Select	ENSP00000415836.2:n.*1274G>C
ENST00000289816.9:c.*1274G>C (ZNF276)	ENSP00000289816.5:n.*1274G>C
ENST00000389301.7:c.3968C>G (FANCA)	ENSP00000373952.3:p.Ala1323Gly
ENST00000561722.5:c.119C>G (FANCA)	ENSP00000456608.1:p.Ala40Gly
ENST00000562424.1:n.239C>G (FANCA)
ENST00000563983.5:n.3107G>C (ZNF276)
ENST00000564475.5:c.298C>G (FANCA)
ENST00000564870.1:c.169C>G (FANCA)
ENST00000564969.5:n.693C>G (FANCA)
ENST00000567879.5:c.413-254C>G (FANCA)	ENSP00000457006.1:n.413-254C>G
ENST00000568369.5:c.3968C>G (FANCA)	ENSP00000456829.1:p.Ala1323Gly
ENST00000568626.1:c.677C>G (FANCA)
NM_000135.2:c.3968C>G , LRG_495t1:c.3968C>G (FANCA)	NP_000126.2:p.Ala1323Gly
NM_001113525.1:c.*1274G>C (ZNF276)	NP_001106997.1:n.*1274G>C
NM_001286167.1:c.3968C>G (FANCA)	NP_001273096.1:p.Ala1323Gly
NM_152287.3:c.*1274G>C (ZNF276)	NP_689500.2:n.*1274G>C
NR_110122.1:n.3291G>C (ZNF276)
NR_110126.1:n.3174G>C (ZNF276)
NR_110128.1:n.3097G>C (ZNF276)
NR_110129.1:n.3186G>C (ZNF276)
XM_005256294.3:c.3968C>G (FANCA)	XP_005256351.1:p.Ala1323Gly
XM_011522945.1:c.3839C>G (FANCA)	XP_011521247.1:p.Ala1280Gly
XM_011522946.1:c.2945C>G (FANCA)	XP_011521248.1:p.Ala982Gly
XM_011522947.1:c.2945C>G (FANCA)	XP_011521249.1:p.Ala982Gly
XR_933244.1:n.3978-231C>G (FANCA)
XR_933245.1:n.3872C>G (FANCA)
NM_000135.3:c.3968C>G (FANCA)	NP_000126.2:p.Ala1323Gly
NM_001286167.2:c.3968C>G (FANCA)	NP_001273096.1:p.Ala1323Gly
XM_005256294.4:c.3968C>G (FANCA)	XP_005256351.1:p.Ala1323Gly
XM_011522945.2:c.3839C>G (FANCA)	XP_011521247.1:p.Ala1280Gly
XM_011522946.3:c.2945C>G (FANCA)	XP_011521248.1:p.Ala982Gly
XM_011522947.2:c.2945C>G (FANCA)	XP_011521249.1:p.Ala982Gly
XM_017023044.2:c.3839C>G (FANCA)	XP_016878533.1:p.Ala1280Gly
XM_017023890.1:c.*1274G>C (ZNF276)	XP_016879379.1:n.*1274G>C
XM_024450189.1:c.2945C>G (FANCA)	XP_024305957.1:p.Ala982Gly
XR_001751866.1:n.3838C>G (FANCA)
XR_933244.2:n.3978-231C>G (FANCA)
XR_933245.2:n.3872C>G (FANCA)
XR_933484.2:n.3285G>C (ZNF276)
NM_000135.4:c.3968C>G (FANCA) MANE Select	NP_000126.2:p.Ala1323Gly
NM_001113525.2:c.*1274G>C (ZNF276) MANE Select	NP_001106997.1:n.*1274G>C
NM_001286167.3:c.3968C>G (FANCA)	NP_001273096.1:p.Ala1323Gly
NM_152287.4:c.*1274G>C (ZNF276)	NP_689500.2:n.*1274G>C
NR_110122.2:n.3274G>C (ZNF276)
NR_110126.2:n.3157G>C (ZNF276)
NR_110129.2:n.3191G>C (ZNF276)
NR_110128.2:n.3097G>C (ZNF276)