Canonical Allele Identifier: CA2133620031

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45175842C= , CM000676.2:g.45175842C=	GRCh38
NC_000014.8:g.45645045C= , CM000676.1:g.45645045C=	GRCh37
NC_000014.7:g.44714795C=	NCBI36
NG_007417.1:g.44910C= , LRG_502:g.44910C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.1300C=	ENSP00000450632.2:p.Arg434=
ENST00000556250.6:c.2881C=	ENSP00000452033.2:p.Arg961=
ENST00000696641.1:c.2929C=	ENSP00000512774.1:p.Arg977=
ENST00000696642.1:c.*1899C=	ENSP00000512775.1:n.*1899C=
ENST00000696646.1:c.*1899C=	ENSP00000512777.1:n.*1899C=
ENST00000696647.1:c.3088C=	ENSP00000512778.1:p.Arg1030=
ENST00000696648.1:c.*1113C=	ENSP00000512779.1:n.*1113C=
ENST00000696649.1:c.2932C=	ENSP00000512780.1:p.Arg978=
ENST00000696650.1:n.3036C=
ENST00000696659.1:c.1086C=
ENST00000696663.1:c.1905C=
ENST00000696664.1:c.1905C=
ENST00000696675.1:c.3088C=	ENSP00000512799.1:p.Arg1030=
ENST00000696683.1:c.1905C=
ENST00000696684.1:c.1905C=
ENST00000696685.1:c.1905C=
ENST00000267430.10:c.3088C= MANE Select	ENSP00000267430.5:p.Arg1030=
ENST00000267430.9:c.3088C=	ENSP00000267430.5:p.Arg1030=
ENST00000542564.6:c.3010C=	ENSP00000442493.2:p.Arg1004=
ENST00000556250.5:c.1636C=	ENSP00000452033.1:p.Arg546=
NM_001308133.1:c.3010C=	NP_001295062.1:p.Arg1004=
NM_020937.2:c.3088C= , LRG_502t1:c.3088C=	NP_065988.1:p.Arg1030=
NM_020937.3:c.3088C=	NP_065988.1:p.Arg1030=
XM_011537034.1:c.3088C=	XP_011535336.1:p.Arg1030=
XM_011537035.1:c.3010C=	XP_011535337.1:p.Arg1004=
XM_011537036.1:c.3088C=	XP_011535338.1:p.Arg1030=
XM_011537037.1:c.1102C=	XP_011535339.1:p.Arg368=
XM_011537034.2:c.3088C=	XP_011535336.1:p.Arg1030=
XM_011537035.3:c.3010C=	XP_011535337.1:p.Arg1004=
XM_011537037.3:c.1102C=	XP_011535339.1:p.Arg368=
XM_017021523.1:c.3088C=	XP_016877012.1:p.Arg1030=
XM_017021524.2:c.2125C=	XP_016877013.1:p.Arg709=
XM_017021525.2:c.1903C=	XP_016877014.1:p.Arg635=
XM_017021526.2:c.1903C=	XP_016877015.1:p.Arg635=
XM_017021527.1:c.1903C=	XP_016877016.1:p.Arg635=
XR_001750470.1:n.3180C=
XR_001750471.2:n.3180C=
XR_001750472.1:n.3180C=
NM_020937.4:c.3088C= MANE Select	NP_065988.1:p.Arg1030=
NM_001308133.2:c.3010C=	NP_001295062.1:p.Arg1004=