Canonical Allele Identifier: CA2133614461

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45166996T= , CM000676.2:g.45166996T=	GRCh38
NC_000014.8:g.45636199T= , CM000676.1:g.45636199T=	GRCh37
NC_000014.7:g.44705949T=	NCBI36
NG_007417.1:g.36064T= , LRG_502:g.36064T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.47T=	ENSP00000450632.2:p.Ile16=
ENST00000556036.6:c.1835T=	ENSP00000450596.1:p.Ile612=
ENST00000556250.6:c.1628T=	ENSP00000452033.2:p.Ile543=
ENST00000696641.1:c.1676T=	ENSP00000512774.1:p.Ile559=
ENST00000696642.1:c.*646T=	ENSP00000512775.1:n.*646T=
ENST00000696646.1:c.*646T=	ENSP00000512777.1:n.*646T=
ENST00000696647.1:c.1835T=	ENSP00000512778.1:p.Ile612=
ENST00000696648.1:c.1835T=	ENSP00000512779.1:p.Ile612=
ENST00000696649.1:c.1835T=	ENSP00000512780.1:p.Ile612=
ENST00000696650.1:n.1783T=
ENST00000696658.1:n.2385T=
ENST00000696662.1:c.1757T=	ENSP00000512788.1:p.Ile586=
ENST00000696663.1:c.652T=
ENST00000696664.1:c.652T=
ENST00000696675.1:c.1835T=	ENSP00000512799.1:p.Ile612=
ENST00000696683.1:c.652T=
ENST00000696684.1:c.652T=
ENST00000696685.1:c.652T=
ENST00000267430.10:c.1835T= MANE Select	ENSP00000267430.5:p.Ile612=
ENST00000267430.9:c.1835T=	ENSP00000267430.5:p.Ile612=
ENST00000542564.6:c.1757T=	ENSP00000442493.2:p.Ile586=
ENST00000556036.5:c.1835T=	ENSP00000450596.1:p.Ile612=
ENST00000556250.5:c.383T=	ENSP00000452033.1:p.Ile128=
NM_001308133.1:c.1757T=	NP_001295062.1:p.Ile586=
NM_001308134.1:c.1835T=	NP_001295063.1:p.Ile612=
NM_020937.2:c.1835T= , LRG_502t1:c.1835T=	NP_065988.1:p.Ile612=
NM_020937.3:c.1835T=	NP_065988.1:p.Ile612=
XM_011537034.1:c.1835T=	XP_011535336.1:p.Ile612=
XM_011537035.1:c.1757T=	XP_011535337.1:p.Ile586=
XM_011537036.1:c.1835T=	XP_011535338.1:p.Ile612=
XM_011537034.2:c.1835T=	XP_011535336.1:p.Ile612=
XM_011537035.3:c.1757T=	XP_011535337.1:p.Ile586=
XM_017021523.1:c.1835T=	XP_016877012.1:p.Ile612=
XM_017021524.2:c.872T=	XP_016877013.1:p.Ile291=
XM_017021525.2:c.650T=	XP_016877014.1:p.Ile217=
XM_017021526.2:c.650T=	XP_016877015.1:p.Ile217=
XM_017021527.1:c.650T=	XP_016877016.1:p.Ile217=
XR_001750470.1:n.1927T=
XR_001750471.2:n.1927T=
XR_001750472.1:n.1927T=
NM_020937.4:c.1835T= MANE Select	NP_065988.1:p.Ile612=
NM_001308133.2:c.1757T=	NP_001295062.1:p.Ile586=
NM_001308134.2:c.1835T=	NP_001295063.1:p.Ile612=