Canonical Allele Identifier: CA389608274

Gene: FANCM

Linked Data

• MyVariant Identifiers: chr14:g.45654514A>G (hg19) ; chr14:g.45185311A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185311A>G , CM000676.2:g.45185311A>G	GRCh38
NC_000014.8:g.45654514A>G , CM000676.1:g.45654514A>G	GRCh37
NC_000014.7:g.44724264A>G	NCBI36
NG_007417.1:g.54379A>G , LRG_502:g.54379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2822A>G	ENSP00000450632.2:p.Glu941Gly
ENST00000555484.2:c.388A>G
ENST00000556250.6:c.4403A>G	ENSP00000452033.2:p.Glu1468Gly
ENST00000557110.2:c.388A>G
ENST00000696642.1:c.*3421A>G	ENSP00000512775.1:n.*3421A>G
ENST00000696644.1:n.346A>G
ENST00000696645.1:n.500A>G
ENST00000696647.1:c.4610A>G	ENSP00000512778.1:p.Glu1537Gly
ENST00000696648.1:c.*2635A>G	ENSP00000512779.1:n.*2635A>G
ENST00000696649.1:c.4454A>G	ENSP00000512780.1:p.Glu1485Gly
ENST00000696650.1:n.4558A>G
ENST00000696659.1:c.2608A>G
ENST00000696663.1:c.3541A>G
ENST00000696664.1:c.3442A>G
ENST00000696665.1:c.388A>G
ENST00000696675.1:c.*366A>G	ENSP00000512799.1:n.*366A>G
ENST00000696683.1:c.3427A>G
ENST00000696684.1:c.3427A>G
ENST00000696685.1:c.3427A>G
ENST00000696686.1:n.1347A>G
ENST00000267430.10:c.4610A>G MANE Select	ENSP00000267430.5:p.Glu1537Gly
ENST00000267430.9:c.4610A>G	ENSP00000267430.5:p.Glu1537Gly
ENST00000542564.6:c.4532A>G	ENSP00000442493.2:p.Glu1511Gly
ENST00000554809.5:c.1407A>G
ENST00000555013.1:n.443A>G
ENST00000556250.5:c.3158A>G	ENSP00000452033.1:p.Glu1053Gly
NM_001308133.1:c.4532A>G	NP_001295062.1:p.Glu1511Gly
NM_020937.2:c.4610A>G , LRG_502t1:c.4610A>G	NP_065988.1:p.Glu1537Gly
NM_020937.3:c.4610A>G	NP_065988.1:p.Glu1537Gly
XM_011537034.1:c.4625A>G	XP_011535336.1:p.Glu1542Gly
XM_011537035.1:c.4547A>G	XP_011535337.1:p.Glu1516Gly
XM_011537036.1:c.4625A>G	XP_011535338.1:p.Glu1542Gly
XM_011537037.1:c.2639A>G	XP_011535339.1:p.Glu880Gly
XM_011537034.2:c.4625A>G	XP_011535336.1:p.Glu1542Gly
XM_011537035.3:c.4547A>G	XP_011535337.1:p.Glu1516Gly
XM_011537037.3:c.2639A>G	XP_011535339.1:p.Glu880Gly
XM_017021523.1:c.4625A>G	XP_016877012.1:p.Glu1542Gly
XM_017021524.2:c.3662A>G	XP_016877013.1:p.Glu1221Gly
XM_017021525.2:c.3440A>G	XP_016877014.1:p.Glu1147Gly
XM_017021526.2:c.3440A>G	XP_016877015.1:p.Glu1147Gly
XM_017021527.1:c.3425A>G	XP_016877016.1:p.Glu1142Gly
XR_001750470.1:n.4717A>G
XR_001750471.2:n.4702A>G
XR_001750472.1:n.4754A>G
NM_020937.4:c.4610A>G MANE Select	NP_065988.1:p.Glu1537Gly
NM_001308133.2:c.4532A>G	NP_001295062.1:p.Glu1511Gly