Canonical Allele Identifier: CA2133624533

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185307A= , CM000676.2:g.45185307A=	GRCh38
NC_000014.8:g.45654510A= , CM000676.1:g.45654510A=	GRCh37
NC_000014.7:g.44724260A=	NCBI36
NG_007417.1:g.54375A= , LRG_502:g.54375A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2818A=	ENSP00000450632.2:p.Asn940=
ENST00000555484.2:c.384A=
ENST00000556250.6:c.4399A=	ENSP00000452033.2:p.Asn1467=
ENST00000557110.2:c.384A=
ENST00000696642.1:c.*3417A=	ENSP00000512775.1:n.*3417A=
ENST00000696644.1:n.342A=
ENST00000696645.1:n.496A=
ENST00000696647.1:c.4606A=	ENSP00000512778.1:p.Asn1536=
ENST00000696648.1:c.*2631A=	ENSP00000512779.1:n.*2631A=
ENST00000696649.1:c.4450A=	ENSP00000512780.1:p.Asn1484=
ENST00000696650.1:n.4554A=
ENST00000696659.1:c.2604A=
ENST00000696663.1:c.3537A=
ENST00000696664.1:c.3438A=
ENST00000696665.1:c.384A=
ENST00000696675.1:c.*362A=	ENSP00000512799.1:n.*362A=
ENST00000696683.1:c.3423A=
ENST00000696684.1:c.3423A=
ENST00000696685.1:c.3423A=
ENST00000696686.1:n.1343A=
ENST00000267430.10:c.4606A= MANE Select	ENSP00000267430.5:p.Asn1536=
ENST00000267430.9:c.4606A=	ENSP00000267430.5:p.Asn1536=
ENST00000542564.6:c.4528A=	ENSP00000442493.2:p.Asn1510=
ENST00000554809.5:c.1403A=
ENST00000555013.1:n.439A=
ENST00000556250.5:c.3154A=	ENSP00000452033.1:p.Asn1052=
NM_001308133.1:c.4528A=	NP_001295062.1:p.Asn1510=
NM_020937.2:c.4606A= , LRG_502t1:c.4606A=	NP_065988.1:p.Asn1536=
NM_020937.3:c.4606A=	NP_065988.1:p.Asn1536=
XM_011537034.1:c.4621A=	XP_011535336.1:p.Asn1541=
XM_011537035.1:c.4543A=	XP_011535337.1:p.Asn1515=
XM_011537036.1:c.4621A=	XP_011535338.1:p.Asn1541=
XM_011537037.1:c.2635A=	XP_011535339.1:p.Asn879=
XM_011537034.2:c.4621A=	XP_011535336.1:p.Asn1541=
XM_011537035.3:c.4543A=	XP_011535337.1:p.Asn1515=
XM_011537037.3:c.2635A=	XP_011535339.1:p.Asn879=
XM_017021523.1:c.4621A=	XP_016877012.1:p.Asn1541=
XM_017021524.2:c.3658A=	XP_016877013.1:p.Asn1220=
XM_017021525.2:c.3436A=	XP_016877014.1:p.Asn1146=
XM_017021526.2:c.3436A=	XP_016877015.1:p.Asn1146=
XM_017021527.1:c.3421A=	XP_016877016.1:p.Asn1141=
XR_001750470.1:n.4713A=
XR_001750471.2:n.4698A=
XR_001750472.1:n.4750A=
NM_020937.4:c.4606A= MANE Select	NP_065988.1:p.Asn1536=
NM_001308133.2:c.4528A=	NP_001295062.1:p.Asn1510=