Canonical Allele Identifier: CA3206810810

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185238G= , CM000676.2:g.45185238G=	GRCh38
NC_000014.8:g.45654441G= , CM000676.1:g.45654441G=	GRCh37
NC_000014.7:g.44724191G=	NCBI36
NG_007417.1:g.54306G= , LRG_502:g.54306G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4537G= MANE Select	NP_065988.1:p.Asp1513=
ENST00000267430.10:c.4537G= MANE Select	ENSP00000267430.5:p.Asp1513=
NM_001308133.1:c.4459G=	NP_001295062.1:p.Asp1487=
NM_001308133.2:c.4459G=	NP_001295062.1:p.Asp1487=
NM_020937.2:c.4537G= , LRG_502t1:c.4537G=	NP_065988.1:p.Asp1513=
NM_020937.3:c.4537G=	NP_065988.1:p.Asp1513=
ENST00000267430.9:c.4537G=	ENSP00000267430.5:p.Asp1513=
ENST00000542564.6:c.4459G=	ENSP00000442493.2:p.Asp1487=
ENST00000554809.5:c.1334G=
ENST00000554809.6:c.2749G=	ENSP00000450632.2:p.Asp917=
ENST00000555013.1:n.370G=
ENST00000555484.2:c.315G=
ENST00000556250.5:c.3085G=	ENSP00000452033.1:p.Asp1029=
ENST00000556250.6:c.4330G=	ENSP00000452033.2:p.Asp1444=
ENST00000557110.2:c.315G=
ENST00000696642.1:c.*3348G=	ENSP00000512775.1:n.*3348G=
ENST00000696644.1:n.273G=
ENST00000696645.1:n.427G=
ENST00000696647.1:c.4537G=	ENSP00000512778.1:p.Asp1513=
ENST00000696648.1:c.*2562G=	ENSP00000512779.1:n.*2562G=
ENST00000696649.1:c.4381G=	ENSP00000512780.1:p.Asp1461=
ENST00000696650.1:n.4485G=
ENST00000696659.1:c.2535G=
ENST00000696663.1:c.3468G=
ENST00000696664.1:c.3369G=
ENST00000696665.1:c.315G=
ENST00000696675.1:c.*293G=	ENSP00000512799.1:n.*293G=
ENST00000696683.1:c.3354G=
ENST00000696684.1:c.3354G=
ENST00000696685.1:c.3354G=
ENST00000696686.1:n.1274G=
XM_011537034.1:c.4552G=	XP_011535336.1:p.Asp1518=
XM_011537034.2:c.4552G=	XP_011535336.1:p.Asp1518=
XM_011537035.1:c.4474G=	XP_011535337.1:p.Asp1492=
XM_011537035.3:c.4474G=	XP_011535337.1:p.Asp1492=
XM_011537036.1:c.4552G=	XP_011535338.1:p.Asp1518=
XM_011537037.1:c.2566G=	XP_011535339.1:p.Asp856=
XM_011537037.3:c.2566G=	XP_011535339.1:p.Asp856=
XM_017021523.1:c.4552G=	XP_016877012.1:p.Asp1518=
XM_017021524.2:c.3589G=	XP_016877013.1:p.Asp1197=
XM_017021525.2:c.3367G=	XP_016877014.1:p.Asp1123=
XM_017021526.2:c.3367G=	XP_016877015.1:p.Asp1123=
XM_017021527.1:c.3352G=	XP_016877016.1:p.Asp1118=
XR_001750470.1:n.4644G=
XR_001750471.2:n.4629G=
XR_001750472.1:n.4681G=