Canonical Allele Identifier: CA2241889454

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738959G= , CM000678.2:g.89738959G=	GRCh38
NC_000016.9:g.89805367G= , CM000678.1:g.89805367G=	GRCh37
NC_000016.8:g.88332868G=	NCBI36
NG_011706.1:g.82699C= , LRG_495:g.82699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2756C= (FANCA)	ENSP00000512522.1:n.*2756C=
ENST00000564475.6:c.4187C= (FANCA)	ENSP00000454977.2:p.Thr1396=
ENST00000567510.2:c.2757C= (FANCA)	ENSP00000455969.1:n.2757C=
ENST00000568369.6:c.4187C= (FANCA)	ENSP00000456829.1:p.Thr1396=
ENST00000696274.1:n.4144C= (FANCA)
ENST00000696275.1:c.*3422C= (FANCA)	ENSP00000512517.1:n.*3422C=
ENST00000696286.1:c.*96C= (FANCA)	ENSP00000512523.1:n.*96C=
ENST00000696287.1:c.4058C= (FANCA)	ENSP00000512524.1:p.Thr1353=
ENST00000696291.1:c.*3615C= (FANCA)	ENSP00000512530.1:n.*3615C=
ENST00000389301.8:c.4183C= (FANCA) MANE Select	ENSP00000373952.3:p.Leu1395=
ENST00000443381.7:c.*713G= (ZNF276) MANE Select	ENSP00000415836.2:n.*713G=
ENST00000289816.9:c.*713G= (ZNF276)	ENSP00000289816.5:n.*713G=
ENST00000389301.7:c.4183C= (FANCA)	ENSP00000373952.3:p.Leu1395=
ENST00000561722.5:c.436-33C= (FANCA)	ENSP00000456608.1:n.436-33C=
ENST00000562424.1:n.454C= (FANCA)
ENST00000563983.5:n.2546G= (ZNF276)
ENST00000564475.5:c.517C= (FANCA)
ENST00000564870.1:c.384C= (FANCA)
ENST00000567879.5:c.557C= (FANCA)	ENSP00000457006.1:p.Thr186=
ENST00000568369.5:c.4187C= (FANCA)	ENSP00000456829.1:p.Thr1396=
NM_000135.2:c.4183C= , LRG_495t1:c.4183C= (FANCA)	NP_000126.2:p.Leu1395=
NM_001113525.1:c.*713G= (ZNF276)	NP_001106997.1:n.*713G=
NM_001286167.1:c.4187C= (FANCA)	NP_001273096.1:p.Thr1396=
NM_152287.3:c.*713G= (ZNF276)	NP_689500.2:n.*713G=
NR_110122.1:n.2730G= (ZNF276)
NR_110126.1:n.2613G= (ZNF276)
NR_110128.1:n.2536G= (ZNF276)
NR_110129.1:n.2625G= (ZNF276)
XM_005256294.3:c.4187C= (FANCA)	XP_005256351.1:p.Thr1396=
XM_011522945.1:c.4058C= (FANCA)	XP_011521247.1:p.Thr1353=
XM_011522946.1:c.3164C= (FANCA)	XP_011521248.1:p.Thr1055=
XM_011522947.1:c.3164C= (FANCA)	XP_011521249.1:p.Thr1055=
XR_933244.1:n.4150C= (FANCA)
XR_933245.1:n.4087C= (FANCA)
NM_000135.3:c.4183C= (FANCA)	NP_000126.2:p.Leu1395=
NM_001286167.2:c.4187C= (FANCA)	NP_001273096.1:p.Thr1396=
XM_005256294.4:c.4187C= (FANCA)	XP_005256351.1:p.Thr1396=
XM_011522945.2:c.4058C= (FANCA)	XP_011521247.1:p.Thr1353=
XM_011522946.3:c.3164C= (FANCA)	XP_011521248.1:p.Thr1055=
XM_011522947.2:c.3164C= (FANCA)	XP_011521249.1:p.Thr1055=
XM_017023044.2:c.4054C= (FANCA)	XP_016878533.1:p.Leu1352=
XM_017023890.1:c.*713G= (ZNF276)	XP_016879379.1:n.*713G=
XM_024450189.1:c.3164C= (FANCA)	XP_024305957.1:p.Thr1055=
XR_933244.2:n.4150C= (FANCA)
XR_933245.2:n.4087C= (FANCA)
XR_933484.2:n.2724G= (ZNF276)
NM_000135.4:c.4183C= (FANCA) MANE Select	NP_000126.2:p.Leu1395=
NM_001113525.2:c.*713G= (ZNF276) MANE Select	NP_001106997.1:n.*713G=
NM_001286167.3:c.4187C= (FANCA)	NP_001273096.1:p.Thr1396=
NM_152287.4:c.*713G= (ZNF276)	NP_689500.2:n.*713G=
NR_110122.2:n.2713G= (ZNF276)
NR_110126.2:n.2596G= (ZNF276)
NR_110129.2:n.2630G= (ZNF276)
NR_110128.2:n.2536G= (ZNF276)