Canonical Allele Identifier: CA397484242

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805537C>G (hg19) ; chr16:g.89739129C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739129C>G , CM000678.2:g.89739129C>G	GRCh38
NC_000016.9:g.89805537C>G , CM000678.1:g.89805537C>G	GRCh37
NC_000016.8:g.88333038C>G	NCBI36
NG_011706.1:g.82529G>C , LRG_495:g.82529G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2740+4G>C (FANCA)	ENSP00000512522.1:n.*2740+4G>C
ENST00000564475.6:c.4171G>C (FANCA)	ENSP00000454977.2:p.Gly1391Arg
ENST00000567510.2:c.2741G>C (FANCA)	ENSP00000455969.1:n.2741G>C
ENST00000568369.6:c.4171G>C (FANCA)	ENSP00000456829.1:p.Gly1391Arg
ENST00000696274.1:n.4128+4G>C (FANCA)
ENST00000696275.1:c.*3406G>C (FANCA)	ENSP00000512517.1:n.*3406G>C
ENST00000696286.1:c.*80+4G>C (FANCA)	ENSP00000512523.1:n.*80+4G>C
ENST00000696287.1:c.4042G>C (FANCA)	ENSP00000512524.1:p.Gly1348Arg
ENST00000696291.1:c.*3599+4G>C (FANCA)	ENSP00000512530.1:n.*3599+4G>C
ENST00000389301.8:c.4167+4G>C (FANCA) MANE Select	ENSP00000373952.3:n.4167+4G>C
ENST00000443381.7:c.*883C>G (ZNF276) MANE Select	ENSP00000415836.2:n.*883C>G
ENST00000289816.9:c.*883C>G (ZNF276)	ENSP00000289816.5:n.*883C>G
ENST00000389301.7:c.4167+4G>C (FANCA)	ENSP00000373952.3:n.4167+4G>C
ENST00000561722.5:c.322G>C (FANCA)	ENSP00000456608.1:p.Gly108Arg
ENST00000562424.1:n.438+4G>C (FANCA)
ENST00000563983.5:n.2716C>G (ZNF276)
ENST00000564475.5:c.501G>C (FANCA)
ENST00000564870.1:c.368+4G>C (FANCA)
ENST00000567879.5:c.541+9G>C (FANCA)	ENSP00000457006.1:n.541+9G>C
ENST00000568369.5:c.4171G>C (FANCA)	ENSP00000456829.1:p.Gly1391Arg
NM_000135.2:c.4167+4G>C , LRG_495t1:c.4167+4G>C (FANCA)	NP_000126.2:n.4167+4G>C
NM_001113525.1:c.*883C>G (ZNF276)	NP_001106997.1:n.*883C>G
NM_001286167.1:c.4171G>C (FANCA)	NP_001273096.1:p.Gly1391Arg
NM_152287.3:c.*883C>G (ZNF276)	NP_689500.2:n.*883C>G
NR_110122.1:n.2900C>G (ZNF276)
NR_110126.1:n.2783C>G (ZNF276)
NR_110128.1:n.2706C>G (ZNF276)
NR_110129.1:n.2795C>G (ZNF276)
XM_005256294.3:c.4171G>C (FANCA)	XP_005256351.1:p.Gly1391Arg
XM_011522945.1:c.4042G>C (FANCA)	XP_011521247.1:p.Gly1348Arg
XM_011522946.1:c.3148G>C (FANCA)	XP_011521248.1:p.Gly1050Arg
XM_011522947.1:c.3148G>C (FANCA)	XP_011521249.1:p.Gly1050Arg
XR_933244.1:n.4134+4G>C (FANCA)
XR_933245.1:n.4071+4G>C (FANCA)
NM_000135.3:c.4167+4G>C (FANCA)	NP_000126.2:n.4167+4G>C
NM_001286167.2:c.4171G>C (FANCA)	NP_001273096.1:p.Gly1391Arg
XM_005256294.4:c.4171G>C (FANCA)	XP_005256351.1:p.Gly1391Arg
XM_011522945.2:c.4042G>C (FANCA)	XP_011521247.1:p.Gly1348Arg
XM_011522946.3:c.3148G>C (FANCA)	XP_011521248.1:p.Gly1050Arg
XM_011522947.2:c.3148G>C (FANCA)	XP_011521249.1:p.Gly1050Arg
XM_017023044.2:c.4038+4G>C (FANCA)	XP_016878533.1:n.4038+4G>C
XM_017023890.1:c.*883C>G (ZNF276)	XP_016879379.1:n.*883C>G
XM_024450189.1:c.3148G>C (FANCA)	XP_024305957.1:p.Gly1050Arg
XR_933244.2:n.4134+4G>C (FANCA)
XR_933245.2:n.4071+4G>C (FANCA)
XR_933484.2:n.2894C>G (ZNF276)
NM_000135.4:c.4167+4G>C (FANCA) MANE Select	NP_000126.2:n.4167+4G>C
NM_001113525.2:c.*883C>G (ZNF276) MANE Select	NP_001106997.1:n.*883C>G
NM_001286167.3:c.4171G>C (FANCA)	NP_001273096.1:p.Gly1391Arg
NM_152287.4:c.*883C>G (ZNF276)	NP_689500.2:n.*883C>G
NR_110122.2:n.2883C>G (ZNF276)
NR_110126.2:n.2766C>G (ZNF276)
NR_110129.2:n.2800C>G (ZNF276)
NR_110128.2:n.2706C>G (ZNF276)