Canonical Allele Identifier: CA486141348

Gene: FANCM

Linked Data

• MyVariant Identifiers: chr14:g.45654452A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185249A>T , CM000676.2:g.45185249A>T	GRCh38
NC_000014.8:g.45654452A>T , CM000676.1:g.45654452A>T	GRCh37
NC_000014.7:g.44724202A>T	NCBI36
NG_007417.1:g.54317A>T , LRG_502:g.54317A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000554809.6:c.2760A>T	ENSP00000450632.2:p.Ala920=
ENST00000555484.2:c.326A>T
ENST00000556250.6:c.4341A>T	ENSP00000452033.2:p.Ala1447=
ENST00000557110.2:c.326A>T
ENST00000696642.1:c.*3359A>T	ENSP00000512775.1:n.*3359A>T
ENST00000696644.1:n.284A>T
ENST00000696645.1:n.438A>T
ENST00000696647.1:c.4548A>T	ENSP00000512778.1:p.Ala1516=
ENST00000696648.1:c.*2573A>T	ENSP00000512779.1:n.*2573A>T
ENST00000696649.1:c.4392A>T	ENSP00000512780.1:p.Ala1464=
ENST00000696650.1:n.4496A>T
ENST00000696659.1:c.2546A>T
ENST00000696663.1:c.3479A>T
ENST00000696664.1:c.3380A>T
ENST00000696665.1:c.326A>T
ENST00000696675.1:c.*304A>T	ENSP00000512799.1:n.*304A>T
ENST00000696683.1:c.3365A>T
ENST00000696684.1:c.3365A>T
ENST00000696685.1:c.3365A>T
ENST00000696686.1:n.1285A>T
ENST00000267430.10:c.4548A>T MANE Select	ENSP00000267430.5:p.Ala1516=
ENST00000267430.9:c.4548A>T	ENSP00000267430.5:p.Ala1516=
ENST00000542564.6:c.4470A>T	ENSP00000442493.2:p.Ala1490=
ENST00000554809.5:c.1345A>T
ENST00000555013.1:n.381A>T
ENST00000556250.5:c.3096A>T	ENSP00000452033.1:p.Ala1032=
NM_001308133.1:c.4470A>T	NP_001295062.1:p.Ala1490=
NM_020937.2:c.4548A>T , LRG_502t1:c.4548A>T	NP_065988.1:p.Ala1516=
NM_020937.3:c.4548A>T	NP_065988.1:p.Ala1516=
XM_011537034.1:c.4563A>T	XP_011535336.1:p.Ala1521=
XM_011537035.1:c.4485A>T	XP_011535337.1:p.Ala1495=
XM_011537036.1:c.4563A>T	XP_011535338.1:p.Ala1521=
XM_011537037.1:c.2577A>T	XP_011535339.1:p.Ala859=
XM_011537034.2:c.4563A>T	XP_011535336.1:p.Ala1521=
XM_011537035.3:c.4485A>T	XP_011535337.1:p.Ala1495=
XM_011537037.3:c.2577A>T	XP_011535339.1:p.Ala859=
XM_017021523.1:c.4563A>T	XP_016877012.1:p.Ala1521=
XM_017021524.2:c.3600A>T	XP_016877013.1:p.Ala1200=
XM_017021525.2:c.3378A>T	XP_016877014.1:p.Ala1126=
XM_017021526.2:c.3378A>T	XP_016877015.1:p.Ala1126=
XM_017021527.1:c.3363A>T	XP_016877016.1:p.Ala1121=
XR_001750470.1:n.4655A>T
XR_001750471.2:n.4640A>T
XR_001750472.1:n.4692A>T
NM_020937.4:c.4548A>T MANE Select	NP_065988.1:p.Ala1516=
NM_001308133.2:c.4470A>T	NP_001295062.1:p.Ala1490=