Canonical Allele Identifier: CA7169734

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45183761C>T , CM000676.2:g.45183761C>T	GRCh38
NC_000014.8:g.45652964C>T , CM000676.1:g.45652964C>T	GRCh37
NC_000014.7:g.44722714C>T	NCBI36
NG_007417.1:g.52829C>T , LRG_502:g.52829C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4387-13C>T MANE Select	NP_065988.1:n.4387-13C>T
ENST00000267430.10:c.4387-13C>T MANE Select	ENSP00000267430.5:n.4387-13C>T
NM_001308133.1:c.4309-13C>T	NP_001295062.1:n.4309-13C>T
NM_001308133.2:c.4309-13C>T	NP_001295062.1:n.4309-13C>T
NM_020937.2:c.4387-13C>T , LRG_502t1:c.4387-13C>T	NP_065988.1:n.4387-13C>T
NM_020937.3:c.4387-13C>T	NP_065988.1:n.4387-13C>T
ENST00000267430.9:c.4387-13C>T	ENSP00000267430.5:n.4387-13C>T
ENST00000542564.6:c.4309-13C>T	ENSP00000442493.2:n.4309-13C>T
ENST00000554809.5:c.1184-13C>T
ENST00000554809.6:c.2599-13C>T	ENSP00000450632.2:n.2599-13C>T
ENST00000555013.1:n.220-13C>T
ENST00000555484.2:c.165-13C>T
ENST00000556250.5:c.2935-13C>T	ENSP00000452033.1:n.2935-13C>T
ENST00000556250.6:c.4180-13C>T	ENSP00000452033.2:n.4180-13C>T
ENST00000557110.2:c.165-13C>T
ENST00000696642.1:c.*3198-13C>T	ENSP00000512775.1:n.*3198-13C>T
ENST00000696644.1:n.123-13C>T
ENST00000696645.1:n.264C>T
ENST00000696647.1:c.4387-13C>T	ENSP00000512778.1:n.4387-13C>T
ENST00000696648.1:c.*2412-13C>T	ENSP00000512779.1:n.*2412-13C>T
ENST00000696649.1:c.4231-13C>T	ENSP00000512780.1:n.4231-13C>T
ENST00000696650.1:n.4335-13C>T
ENST00000696659.1:c.2385-13C>T
ENST00000696663.1:c.3318-13C>T
ENST00000696664.1:c.3219-13C>T
ENST00000696665.1:c.165-13C>T
ENST00000696675.1:c.*143-13C>T	ENSP00000512799.1:n.*143-13C>T
ENST00000696683.1:c.3204-13C>T
ENST00000696684.1:c.3204-13C>T
ENST00000696685.1:c.3204-13C>T
ENST00000696686.1:n.1124-13C>T
XM_011537034.1:c.4402-13C>T	XP_011535336.1:n.4402-13C>T
XM_011537034.2:c.4402-13C>T	XP_011535336.1:n.4402-13C>T
XM_011537035.1:c.4324-13C>T	XP_011535337.1:n.4324-13C>T
XM_011537035.3:c.4324-13C>T	XP_011535337.1:n.4324-13C>T
XM_011537036.1:c.4402-13C>T	XP_011535338.1:n.4402-13C>T
XM_011537037.1:c.2416-13C>T	XP_011535339.1:n.2416-13C>T
XM_011537037.3:c.2416-13C>T	XP_011535339.1:n.2416-13C>T
XM_017021523.1:c.4402-13C>T	XP_016877012.1:n.4402-13C>T
XM_017021524.2:c.3439-13C>T	XP_016877013.1:n.3439-13C>T
XM_017021525.2:c.3217-13C>T	XP_016877014.1:n.3217-13C>T
XM_017021526.2:c.3217-13C>T	XP_016877015.1:n.3217-13C>T
XM_017021527.1:c.3202-13C>T	XP_016877016.1:n.3202-13C>T
XR_001750470.1:n.4494-13C>T
XR_001750471.2:n.4479-13C>T
XR_001750472.1:n.4531-13C>T