Canonical Allele Identifier: CA2133613587

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154724G= , CM000676.2:g.45154724G=	GRCh38
NC_000014.8:g.45623927G= , CM000676.1:g.45623927G=	GRCh37
NC_000014.7:g.44693677G=	NCBI36
NG_007417.1:g.23792G= , LRG_502:g.23792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1211G=	ENSP00000450596.1:p.Gly404=
ENST00000556250.6:c.1211G=	ENSP00000452033.2:p.Gly404=
ENST00000696641.1:c.1052G=	ENSP00000512774.1:p.Gly351=
ENST00000696642.1:c.*22G=	ENSP00000512775.1:n.*22G=
ENST00000696643.1:c.1211G=	ENSP00000512776.1:p.Gly404=
ENST00000696646.1:c.*22G=	ENSP00000512777.1:n.*22G=
ENST00000696647.1:c.1211G=	ENSP00000512778.1:p.Gly404=
ENST00000696648.1:c.1211G=	ENSP00000512779.1:p.Gly404=
ENST00000696649.1:c.1211G=	ENSP00000512780.1:p.Gly404=
ENST00000696650.1:n.1159G=
ENST00000696657.1:c.*429G=	ENSP00000512784.1:n.*429G=
ENST00000696658.1:n.1761G=
ENST00000696662.1:c.1133G=	ENSP00000512788.1:p.Gly378=
ENST00000696663.1:c.28G=
ENST00000696664.1:c.28G=
ENST00000696675.1:c.1211G=	ENSP00000512799.1:p.Gly404=
ENST00000696680.1:c.1079G=	ENSP00000512803.1:p.Gly360=
ENST00000696681.1:c.*22G=	ENSP00000512804.1:n.*22G=
ENST00000696682.1:c.1211G=	ENSP00000512805.1:p.Gly404=
ENST00000696683.1:c.28G=
ENST00000696684.1:c.28G=
ENST00000696685.1:c.28G=
ENST00000267430.10:c.1211G= MANE Select	ENSP00000267430.5:p.Gly404=
ENST00000267430.9:c.1211G=	ENSP00000267430.5:p.Gly404=
ENST00000542564.6:c.1133G=	ENSP00000442493.2:p.Gly378=
ENST00000556036.5:c.1211G=	ENSP00000450596.1:p.Gly404=
NM_001308133.1:c.1133G=	NP_001295062.1:p.Gly378=
NM_001308134.1:c.1211G=	NP_001295063.1:p.Gly404=
NM_020937.2:c.1211G= , LRG_502t1:c.1211G=	NP_065988.1:p.Gly404=
NM_020937.3:c.1211G=	NP_065988.1:p.Gly404=
XM_011537034.1:c.1211G=	XP_011535336.1:p.Gly404=
XM_011537035.1:c.1133G=	XP_011535337.1:p.Gly378=
XM_011537036.1:c.1211G=	XP_011535338.1:p.Gly404=
XM_011537034.2:c.1211G=	XP_011535336.1:p.Gly404=
XM_011537035.3:c.1133G=	XP_011535337.1:p.Gly378=
XM_017021523.1:c.1211G=	XP_016877012.1:p.Gly404=
XM_017021524.2:c.248G=	XP_016877013.1:p.Gly83=
XM_017021525.2:c.26G=	XP_016877014.1:p.Gly9=
XM_017021526.2:c.26G=	XP_016877015.1:p.Gly9=
XM_017021527.1:c.26G=	XP_016877016.1:p.Gly9=
XR_001750470.1:n.1303G=
XR_001750471.2:n.1303G=
XR_001750472.1:n.1303G=
NM_020937.4:c.1211G= MANE Select	NP_065988.1:p.Gly404=
NM_001308133.2:c.1133G=	NP_001295062.1:p.Gly378=
NM_001308134.2:c.1211G=	NP_001295063.1:p.Gly404=