Canonical Allele Identifier: CA2241889588

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739157G= , CM000678.2:g.89739157G=	GRCh38
NC_000016.9:g.89805565G= , CM000678.1:g.89805565G=	GRCh37
NC_000016.8:g.88333066G=	NCBI36
NG_011706.1:g.82501C= , LRG_495:g.82501C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2716C= (FANCA)	ENSP00000512522.1:n.*2716C=
ENST00000564475.6:c.4143C= (FANCA)	ENSP00000454977.2:p.Gly1381=
ENST00000567510.2:c.2713C= (FANCA)	ENSP00000455969.1:n.2713C=
ENST00000568369.6:c.4143C= (FANCA)	ENSP00000456829.1:p.Gly1381=
ENST00000696274.1:n.4104C= (FANCA)
ENST00000696275.1:c.*3378C= (FANCA)	ENSP00000512517.1:n.*3378C=
ENST00000696286.1:c.*56C= (FANCA)	ENSP00000512523.1:n.*56C=
ENST00000696287.1:c.4014C= (FANCA)	ENSP00000512524.1:p.Gly1338=
ENST00000696291.1:c.*3575C= (FANCA)	ENSP00000512530.1:n.*3575C=
ENST00000389301.8:c.4143C= (FANCA) MANE Select	ENSP00000373952.3:p.Gly1381=
ENST00000443381.7:c.*911G= (ZNF276) MANE Select	ENSP00000415836.2:n.*911G=
ENST00000289816.9:c.*911G= (ZNF276)	ENSP00000289816.5:n.*911G=
ENST00000389301.7:c.4143C= (FANCA)	ENSP00000373952.3:p.Gly1381=
ENST00000561722.5:c.294C= (FANCA)	ENSP00000456608.1:p.Gly98=
ENST00000562424.1:n.414C= (FANCA)
ENST00000563983.5:n.2744G= (ZNF276)
ENST00000564475.5:c.473C= (FANCA)
ENST00000564870.1:c.344C= (FANCA)
ENST00000567879.5:c.522C= (FANCA)	ENSP00000457006.1:p.Gly174=
ENST00000568369.5:c.4143C= (FANCA)	ENSP00000456829.1:p.Gly1381=
NM_000135.2:c.4143C= , LRG_495t1:c.4143C= (FANCA)	NP_000126.2:p.Gly1381=
NM_001113525.1:c.*911G= (ZNF276)	NP_001106997.1:n.*911G=
NM_001286167.1:c.4143C= (FANCA)	NP_001273096.1:p.Gly1381=
NM_152287.3:c.*911G= (ZNF276)	NP_689500.2:n.*911G=
NR_110122.1:n.2928G= (ZNF276)
NR_110126.1:n.2811G= (ZNF276)
NR_110128.1:n.2734G= (ZNF276)
NR_110129.1:n.2823G= (ZNF276)
XM_005256294.3:c.4143C= (FANCA)	XP_005256351.1:p.Gly1381=
XM_011522945.1:c.4014C= (FANCA)	XP_011521247.1:p.Gly1338=
XM_011522946.1:c.3120C= (FANCA)	XP_011521248.1:p.Gly1040=
XM_011522947.1:c.3120C= (FANCA)	XP_011521249.1:p.Gly1040=
XR_933244.1:n.4110C= (FANCA)
XR_933245.1:n.4047C= (FANCA)
NM_000135.3:c.4143C= (FANCA)	NP_000126.2:p.Gly1381=
NM_001286167.2:c.4143C= (FANCA)	NP_001273096.1:p.Gly1381=
XM_005256294.4:c.4143C= (FANCA)	XP_005256351.1:p.Gly1381=
XM_011522945.2:c.4014C= (FANCA)	XP_011521247.1:p.Gly1338=
XM_011522946.3:c.3120C= (FANCA)	XP_011521248.1:p.Gly1040=
XM_011522947.2:c.3120C= (FANCA)	XP_011521249.1:p.Gly1040=
XM_017023044.2:c.4014C= (FANCA)	XP_016878533.1:p.Gly1338=
XM_017023890.1:c.*911G= (ZNF276)	XP_016879379.1:n.*911G=
XM_024450189.1:c.3120C= (FANCA)	XP_024305957.1:p.Gly1040=
XR_933244.2:n.4110C= (FANCA)
XR_933245.2:n.4047C= (FANCA)
XR_933484.2:n.2922G= (ZNF276)
NM_000135.4:c.4143C= (FANCA) MANE Select	NP_000126.2:p.Gly1381=
NM_001113525.2:c.*911G= (ZNF276) MANE Select	NP_001106997.1:n.*911G=
NM_001286167.3:c.4143C= (FANCA)	NP_001273096.1:p.Gly1381=
NM_152287.4:c.*911G= (ZNF276)	NP_689500.2:n.*911G=
NR_110122.2:n.2911G= (ZNF276)
NR_110126.2:n.2794G= (ZNF276)
NR_110129.2:n.2828G= (ZNF276)
NR_110128.2:n.2734G= (ZNF276)