Canonical Allele Identifier: CA2241906918

Gene: FANCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89764878A= , CM000678.2:g.89764878A=	GRCh38
NC_000016.9:g.89831286A= , CM000678.1:g.89831286A=	GRCh37
NC_000016.8:g.88358787A=	NCBI36
NG_011706.1:g.56780T= , LRG_495:g.56780T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*1272+12T=	ENSP00000512522.1:n.*1272+12T=
ENST00000564475.6:c.2778+12T=	ENSP00000454977.2:n.2778+12T=
ENST00000567510.2:c.1477+12T=	ENSP00000455969.1:n.1477+12T=
ENST00000568369.6:c.2778+12T=	ENSP00000456829.1:n.2778+12T=
ENST00000696274.1:n.2739+12T=
ENST00000696275.1:c.*2013+12T=	ENSP00000512517.1:n.*2013+12T=
ENST00000696276.1:n.2821+12T=
ENST00000696286.1:c.2778+12T=	ENSP00000512523.1:n.2778+12T=
ENST00000696287.1:c.2778+12T=	ENSP00000512524.1:n.2778+12T=
ENST00000696291.1:c.*2498+12T=	ENSP00000512530.1:n.*2498+12T=
ENST00000389301.8:c.2778+12T= MANE Select	ENSP00000373952.3:n.2778+12T=
ENST00000305699.15:n.150+12T=
ENST00000389301.7:c.2778+12T=	ENSP00000373952.3:n.2778+12T=
ENST00000561660.1:c.155+12T=
ENST00000563318.1:c.184+12T=
ENST00000563510.5:c.70T=
ENST00000567988.5:c.115+12T=
ENST00000568369.5:c.2778+12T=	ENSP00000456829.1:n.2778+12T=
NM_000135.2:c.2778+12T= , LRG_495t1:c.2778+12T=	NP_000126.2:n.2778+12T=
NM_001286167.1:c.2778+12T=	NP_001273096.1:n.2778+12T=
XM_005256294.3:c.2778+12T=	XP_005256351.1:n.2778+12T=
XM_011522945.1:c.2778+12T=	XP_011521247.1:n.2778+12T=
XM_011522946.1:c.1755+12T=	XP_011521248.1:n.1755+12T=
XM_011522947.1:c.1755+12T=	XP_011521249.1:n.1755+12T=
XR_933244.1:n.2821+12T=
XR_933245.1:n.2821+12T=
XR_933246.1:n.2821+12T=
NM_000135.3:c.2778+12T=	NP_000126.2:n.2778+12T=
NM_001286167.2:c.2778+12T=	NP_001273096.1:n.2778+12T=
XM_005256294.4:c.2778+12T=	XP_005256351.1:n.2778+12T=
XM_011522945.2:c.2778+12T=	XP_011521247.1:n.2778+12T=
XM_011522946.3:c.1755+12T=	XP_011521248.1:n.1755+12T=
XM_011522947.2:c.1755+12T=	XP_011521249.1:n.1755+12T=
XM_017023044.2:c.2778+12T=	XP_016878533.1:n.2778+12T=
XM_017023045.1:c.2778+12T=	XP_016878534.1:n.2778+12T=
XM_024450189.1:c.1755+12T=	XP_024305957.1:n.1755+12T=
XR_001751866.1:n.2821+12T=
XR_933244.2:n.2821+12T=
XR_933245.2:n.2821+12T=
XR_933247.2:n.2950+12T=
NM_000135.4:c.2778+12T= MANE Select	NP_000126.2:n.2778+12T=
NM_001286167.3:c.2778+12T=	NP_001273096.1:n.2778+12T=