Canonical Allele Identifier: CA486141361

Gene: FANCM

Linked Data

• gnomAD v4: 14-45185273-A-G
• MyVariant Identifiers: chr14:g.45654476A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185273A>G , CM000676.2:g.45185273A>G	GRCh38
NC_000014.8:g.45654476A>G , CM000676.1:g.45654476A>G	GRCh37
NC_000014.7:g.44724226A>G	NCBI36
NG_007417.1:g.54341A>G , LRG_502:g.54341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2784A>G	ENSP00000450632.2:p.Glu928=
ENST00000555484.2:c.350A>G
ENST00000556250.6:c.4365A>G	ENSP00000452033.2:p.Glu1455=
ENST00000557110.2:c.350A>G
ENST00000696642.1:c.*3383A>G	ENSP00000512775.1:n.*3383A>G
ENST00000696644.1:n.308A>G
ENST00000696645.1:n.462A>G
ENST00000696647.1:c.4572A>G	ENSP00000512778.1:p.Glu1524=
ENST00000696648.1:c.*2597A>G	ENSP00000512779.1:n.*2597A>G
ENST00000696649.1:c.4416A>G	ENSP00000512780.1:p.Glu1472=
ENST00000696650.1:n.4520A>G
ENST00000696659.1:c.2570A>G
ENST00000696663.1:c.3503A>G
ENST00000696664.1:c.3404A>G
ENST00000696665.1:c.350A>G
ENST00000696675.1:c.*328A>G	ENSP00000512799.1:n.*328A>G
ENST00000696683.1:c.3389A>G
ENST00000696684.1:c.3389A>G
ENST00000696685.1:c.3389A>G
ENST00000696686.1:n.1309A>G
ENST00000267430.10:c.4572A>G MANE Select	ENSP00000267430.5:p.Glu1524=
ENST00000267430.9:c.4572A>G	ENSP00000267430.5:p.Glu1524=
ENST00000542564.6:c.4494A>G	ENSP00000442493.2:p.Glu1498=
ENST00000554809.5:c.1369A>G
ENST00000555013.1:n.405A>G
ENST00000556250.5:c.3120A>G	ENSP00000452033.1:p.Glu1040=
NM_001308133.1:c.4494A>G	NP_001295062.1:p.Glu1498=
NM_020937.2:c.4572A>G , LRG_502t1:c.4572A>G	NP_065988.1:p.Glu1524=
NM_020937.3:c.4572A>G	NP_065988.1:p.Glu1524=
XM_011537034.1:c.4587A>G	XP_011535336.1:p.Glu1529=
XM_011537035.1:c.4509A>G	XP_011535337.1:p.Glu1503=
XM_011537036.1:c.4587A>G	XP_011535338.1:p.Glu1529=
XM_011537037.1:c.2601A>G	XP_011535339.1:p.Glu867=
XM_011537034.2:c.4587A>G	XP_011535336.1:p.Glu1529=
XM_011537035.3:c.4509A>G	XP_011535337.1:p.Glu1503=
XM_011537037.3:c.2601A>G	XP_011535339.1:p.Glu867=
XM_017021523.1:c.4587A>G	XP_016877012.1:p.Glu1529=
XM_017021524.2:c.3624A>G	XP_016877013.1:p.Glu1208=
XM_017021525.2:c.3402A>G	XP_016877014.1:p.Glu1134=
XM_017021526.2:c.3402A>G	XP_016877015.1:p.Glu1134=
XM_017021527.1:c.3387A>G	XP_016877016.1:p.Glu1129=
XR_001750470.1:n.4679A>G
XR_001750471.2:n.4664A>G
XR_001750472.1:n.4716A>G
NM_020937.4:c.4572A>G MANE Select	NP_065988.1:p.Glu1524=
NM_001308133.2:c.4494A>G	NP_001295062.1:p.Glu1498=