Canonical Allele Identifier: CA2241896050

Gene: FANCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89744960C= , CM000678.2:g.89744960C=	GRCh38
NC_000016.9:g.89811368C= , CM000678.1:g.89811368C=	GRCh37
NC_000016.8:g.88338869C=	NCBI36
NG_011706.1:g.76698G= , LRG_495:g.76698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2103G=	ENSP00000512522.1:n.*2103G=
ENST00000564475.6:c.3625G=	ENSP00000454977.2:p.Asp1209=
ENST00000567510.2:c.2195G=	ENSP00000455969.1:n.2195G=
ENST00000568369.6:c.3625G=	ENSP00000456829.1:p.Asp1209=
ENST00000568983.6:n.644G=
ENST00000696274.1:n.3586G=
ENST00000696275.1:c.*2860G=	ENSP00000512517.1:n.*2860G=
ENST00000696286.1:c.3625G=	ENSP00000512523.1:p.Asp1209=
ENST00000696287.1:c.3496G=	ENSP00000512524.1:p.Asp1166=
ENST00000696291.1:c.*3057G=	ENSP00000512530.1:n.*3057G=
ENST00000389301.8:c.3625G= MANE Select	ENSP00000373952.3:p.Asp1209=
ENST00000305699.15:n.868G=
ENST00000389301.7:c.3625G=	ENSP00000373952.3:p.Asp1209=
ENST00000564969.5:n.49G=
ENST00000567879.5:c.103G=	ENSP00000457006.1:p.Asp35=
ENST00000567988.5:c.877G=
ENST00000568369.5:c.3625G=	ENSP00000456829.1:p.Asp1209=
ENST00000568626.1:c.473G=
ENST00000568983.5:n.453G=
NM_000135.2:c.3625G= , LRG_495t1:c.3625G=	NP_000126.2:p.Asp1209=
NM_001286167.1:c.3625G=	NP_001273096.1:p.Asp1209=
XM_005256294.3:c.3625G=	XP_005256351.1:p.Asp1209=
XM_011522945.1:c.3496G=	XP_011521247.1:p.Asp1166=
XM_011522946.1:c.2602G=	XP_011521248.1:p.Asp868=
XM_011522947.1:c.2602G=	XP_011521249.1:p.Asp868=
XR_933244.1:n.3668G=
XR_933245.1:n.3668G=
XR_933246.1:n.3495G=
NM_000135.3:c.3625G=	NP_000126.2:p.Asp1209=
NM_001286167.2:c.3625G=	NP_001273096.1:p.Asp1209=
XM_005256294.4:c.3625G=	XP_005256351.1:p.Asp1209=
XM_011522945.2:c.3496G=	XP_011521247.1:p.Asp1166=
XM_011522946.3:c.2602G=	XP_011521248.1:p.Asp868=
XM_011522947.2:c.2602G=	XP_011521249.1:p.Asp868=
XM_017023044.2:c.3496G=	XP_016878533.1:p.Asp1166=
XM_024450189.1:c.2602G=	XP_024305957.1:p.Asp868=
XR_001751866.1:n.3495G=
XR_933244.2:n.3668G=
XR_933245.2:n.3668G=
NM_000135.4:c.3625G= MANE Select	NP_000126.2:p.Asp1209=
NM_001286167.3:c.3625G=	NP_001273096.1:p.Asp1209=