Canonical Allele Identifier: CA486141394

Gene: FANCM

Linked Data

• MyVariant Identifiers: chr14:g.45654527A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185324A>T , CM000676.2:g.45185324A>T	GRCh38
NC_000014.8:g.45654527A>T , CM000676.1:g.45654527A>T	GRCh37
NC_000014.7:g.44724277A>T	NCBI36
NG_007417.1:g.54392A>T , LRG_502:g.54392A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2835A>T	ENSP00000450632.2:p.Ser945=
ENST00000555484.2:c.401A>T
ENST00000556250.6:c.4416A>T	ENSP00000452033.2:p.Ser1472=
ENST00000557110.2:c.401A>T
ENST00000696642.1:c.*3434A>T	ENSP00000512775.1:n.*3434A>T
ENST00000696644.1:n.359A>T
ENST00000696645.1:n.513A>T
ENST00000696647.1:c.4623A>T	ENSP00000512778.1:p.Ser1541=
ENST00000696648.1:c.*2648A>T	ENSP00000512779.1:n.*2648A>T
ENST00000696649.1:c.4467A>T	ENSP00000512780.1:p.Ser1489=
ENST00000696650.1:n.4571A>T
ENST00000696659.1:c.2621A>T
ENST00000696663.1:c.3554A>T
ENST00000696664.1:c.3455A>T
ENST00000696665.1:c.401A>T
ENST00000696675.1:c.*379A>T	ENSP00000512799.1:n.*379A>T
ENST00000696683.1:c.3440A>T
ENST00000696684.1:c.3440A>T
ENST00000696685.1:c.3440A>T
ENST00000696686.1:n.1360A>T
ENST00000267430.10:c.4623A>T MANE Select	ENSP00000267430.5:p.Ser1541=
ENST00000267430.9:c.4623A>T	ENSP00000267430.5:p.Ser1541=
ENST00000542564.6:c.4545A>T	ENSP00000442493.2:p.Ser1515=
ENST00000554809.5:c.1420A>T
ENST00000555013.1:n.456A>T
ENST00000556250.5:c.3171A>T	ENSP00000452033.1:p.Ser1057=
NM_001308133.1:c.4545A>T	NP_001295062.1:p.Ser1515=
NM_020937.2:c.4623A>T , LRG_502t1:c.4623A>T	NP_065988.1:p.Ser1541=
NM_020937.3:c.4623A>T	NP_065988.1:p.Ser1541=
XM_011537034.1:c.4638A>T	XP_011535336.1:p.Ser1546=
XM_011537035.1:c.4560A>T	XP_011535337.1:p.Ser1520=
XM_011537036.1:c.4638A>T	XP_011535338.1:p.Ser1546=
XM_011537037.1:c.2652A>T	XP_011535339.1:p.Ser884=
XM_011537034.2:c.4638A>T	XP_011535336.1:p.Ser1546=
XM_011537035.3:c.4560A>T	XP_011535337.1:p.Ser1520=
XM_011537037.3:c.2652A>T	XP_011535339.1:p.Ser884=
XM_017021523.1:c.4638A>T	XP_016877012.1:p.Ser1546=
XM_017021524.2:c.3675A>T	XP_016877013.1:p.Ser1225=
XM_017021525.2:c.3453A>T	XP_016877014.1:p.Ser1151=
XM_017021526.2:c.3453A>T	XP_016877015.1:p.Ser1151=
XM_017021527.1:c.3438A>T	XP_016877016.1:p.Ser1146=
XR_001750470.1:n.4730A>T
XR_001750471.2:n.4715A>T
XR_001750472.1:n.4767A>T
NM_020937.4:c.4623A>T MANE Select	NP_065988.1:p.Ser1541=
NM_001308133.2:c.4545A>T	NP_001295062.1:p.Ser1515=