Canonical Allele Identifier: CA2241889602

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739176G= , CM000678.2:g.89739176G=	GRCh38
NC_000016.9:g.89805584G= , CM000678.1:g.89805584G=	GRCh37
NC_000016.8:g.88333085G=	NCBI36
NG_011706.1:g.82482C= , LRG_495:g.82482C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2697C= (FANCA)	ENSP00000512522.1:n.*2697C=
ENST00000564475.6:c.4124C= (FANCA)	ENSP00000454977.2:p.Thr1375=
ENST00000567510.2:c.2694C= (FANCA)	ENSP00000455969.1:n.2694C=
ENST00000568369.6:c.4124C= (FANCA)	ENSP00000456829.1:p.Thr1375=
ENST00000696274.1:n.4085C= (FANCA)
ENST00000696275.1:c.*3359C= (FANCA)	ENSP00000512517.1:n.*3359C=
ENST00000696286.1:c.*37C= (FANCA)	ENSP00000512523.1:n.*37C=
ENST00000696287.1:c.3995C= (FANCA)	ENSP00000512524.1:p.Thr1332=
ENST00000696291.1:c.*3556C= (FANCA)	ENSP00000512530.1:n.*3556C=
ENST00000389301.8:c.4124C= (FANCA) MANE Select	ENSP00000373952.3:p.Thr1375=
ENST00000443381.7:c.*930G= (ZNF276) MANE Select	ENSP00000415836.2:n.*930G=
ENST00000289816.9:c.*930G= (ZNF276)	ENSP00000289816.5:n.*930G=
ENST00000389301.7:c.4124C= (FANCA)	ENSP00000373952.3:p.Thr1375=
ENST00000561722.5:c.275C= (FANCA)	ENSP00000456608.1:p.Thr92=
ENST00000562424.1:n.395C= (FANCA)
ENST00000563983.5:n.2763G= (ZNF276)
ENST00000564475.5:c.454C= (FANCA)
ENST00000564870.1:c.325C= (FANCA)
ENST00000567879.5:c.503C= (FANCA)	ENSP00000457006.1:p.Thr168=
ENST00000568369.5:c.4124C= (FANCA)	ENSP00000456829.1:p.Thr1375=
NM_000135.2:c.4124C= , LRG_495t1:c.4124C= (FANCA)	NP_000126.2:p.Thr1375=
NM_001113525.1:c.*930G= (ZNF276)	NP_001106997.1:n.*930G=
NM_001286167.1:c.4124C= (FANCA)	NP_001273096.1:p.Thr1375=
NM_152287.3:c.*930G= (ZNF276)	NP_689500.2:n.*930G=
NR_110122.1:n.2947G= (ZNF276)
NR_110126.1:n.2830G= (ZNF276)
NR_110128.1:n.2753G= (ZNF276)
NR_110129.1:n.2842G= (ZNF276)
XM_005256294.3:c.4124C= (FANCA)	XP_005256351.1:p.Thr1375=
XM_011522945.1:c.3995C= (FANCA)	XP_011521247.1:p.Thr1332=
XM_011522946.1:c.3101C= (FANCA)	XP_011521248.1:p.Thr1034=
XM_011522947.1:c.3101C= (FANCA)	XP_011521249.1:p.Thr1034=
XR_933244.1:n.4091C= (FANCA)
XR_933245.1:n.4028C= (FANCA)
NM_000135.3:c.4124C= (FANCA)	NP_000126.2:p.Thr1375=
NM_001286167.2:c.4124C= (FANCA)	NP_001273096.1:p.Thr1375=
XM_005256294.4:c.4124C= (FANCA)	XP_005256351.1:p.Thr1375=
XM_011522945.2:c.3995C= (FANCA)	XP_011521247.1:p.Thr1332=
XM_011522946.3:c.3101C= (FANCA)	XP_011521248.1:p.Thr1034=
XM_011522947.2:c.3101C= (FANCA)	XP_011521249.1:p.Thr1034=
XM_017023044.2:c.3995C= (FANCA)	XP_016878533.1:p.Thr1332=
XM_017023890.1:c.*930G= (ZNF276)	XP_016879379.1:n.*930G=
XM_024450189.1:c.3101C= (FANCA)	XP_024305957.1:p.Thr1034=
XR_933244.2:n.4091C= (FANCA)
XR_933245.2:n.4028C= (FANCA)
XR_933484.2:n.2941G= (ZNF276)
NM_000135.4:c.4124C= (FANCA) MANE Select	NP_000126.2:p.Thr1375=
NM_001113525.2:c.*930G= (ZNF276) MANE Select	NP_001106997.1:n.*930G=
NM_001286167.3:c.4124C= (FANCA)	NP_001273096.1:p.Thr1375=
NM_152287.4:c.*930G= (ZNF276)	NP_689500.2:n.*930G=
NR_110122.2:n.2930G= (ZNF276)
NR_110126.2:n.2813G= (ZNF276)
NR_110129.2:n.2847G= (ZNF276)
NR_110128.2:n.2753G= (ZNF276)