Canonical Allele Identifier: CA259618802

Gene: FANCM

Linked Data

• dbSNP Id: rs373430198
• MyVariant Identifiers: chr14:g.45628484G>T (hg19) ; chr14:g.45159281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159281G>T , CM000676.2:g.45159281G>T	GRCh38
NC_000014.8:g.45628484G>T , CM000676.1:g.45628484G>T	GRCh37
NC_000014.7:g.44698234G>T	NCBI36
NG_007417.1:g.28349G>T , LRG_502:g.28349G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1581+1G>T	ENSP00000450596.1:n.1581+1G>T
ENST00000556250.6:c.1581+1G>T	ENSP00000452033.2:n.1581+1G>T
ENST00000696641.1:c.1422+1G>T	ENSP00000512774.1:n.1422+1G>T
ENST00000696642.1:c.*392+1G>T	ENSP00000512775.1:n.*392+1G>T
ENST00000696643.1:c.1582G>T	ENSP00000512776.1:p.Val528Leu
ENST00000696646.1:c.*392+1G>T	ENSP00000512777.1:n.*392+1G>T
ENST00000696647.1:c.1581+1G>T	ENSP00000512778.1:n.1581+1G>T
ENST00000696648.1:c.1581+1G>T	ENSP00000512779.1:n.1581+1G>T
ENST00000696649.1:c.1581+1G>T	ENSP00000512780.1:n.1581+1G>T
ENST00000696650.1:n.1529+1G>T
ENST00000696658.1:n.2131+1G>T
ENST00000696662.1:c.1503+1G>T	ENSP00000512788.1:n.1503+1G>T
ENST00000696663.1:c.398+1G>T
ENST00000696664.1:c.398+1G>T
ENST00000696675.1:c.1581+1G>T	ENSP00000512799.1:n.1581+1G>T
ENST00000696681.1:c.*393G>T	ENSP00000512804.1:n.*393G>T
ENST00000696682.1:c.1581+1G>T	ENSP00000512805.1:n.1581+1G>T
ENST00000696683.1:c.398+1G>T
ENST00000696684.1:c.398+1G>T
ENST00000696685.1:c.398+1G>T
ENST00000267430.10:c.1581+1G>T MANE Select	ENSP00000267430.5:n.1581+1G>T
ENST00000267430.9:c.1581+1G>T	ENSP00000267430.5:n.1581+1G>T
ENST00000542564.6:c.1503+1G>T	ENSP00000442493.2:n.1503+1G>T
ENST00000556036.5:c.1581+1G>T	ENSP00000450596.1:n.1581+1G>T
ENST00000556250.5:c.336+1G>T	ENSP00000452033.1:n.336+1G>T
NM_001308133.1:c.1503+1G>T	NP_001295062.1:n.1503+1G>T
NM_001308134.1:c.1581+1G>T	NP_001295063.1:n.1581+1G>T
NM_020937.2:c.1581+1G>T , LRG_502t1:c.1581+1G>T	NP_065988.1:n.1581+1G>T
NM_020937.3:c.1581+1G>T	NP_065988.1:n.1581+1G>T
XM_011537034.1:c.1581+1G>T	XP_011535336.1:n.1581+1G>T
XM_011537035.1:c.1503+1G>T	XP_011535337.1:n.1503+1G>T
XM_011537036.1:c.1581+1G>T	XP_011535338.1:n.1581+1G>T
XM_011537034.2:c.1581+1G>T	XP_011535336.1:n.1581+1G>T
XM_011537035.3:c.1503+1G>T	XP_011535337.1:n.1503+1G>T
XM_017021523.1:c.1581+1G>T	XP_016877012.1:n.1581+1G>T
XM_017021524.2:c.618+1G>T	XP_016877013.1:n.618+1G>T
XM_017021525.2:c.396+1G>T	XP_016877014.1:n.396+1G>T
XM_017021526.2:c.396+1G>T	XP_016877015.1:n.396+1G>T
XM_017021527.1:c.396+1G>T	XP_016877016.1:n.396+1G>T
XR_001750470.1:n.1673+1G>T
XR_001750471.2:n.1673+1G>T
XR_001750472.1:n.1673+1G>T
NM_020937.4:c.1581+1G>T MANE Select	NP_065988.1:n.1581+1G>T
NM_001308133.2:c.1503+1G>T	NP_001295062.1:n.1503+1G>T
NM_001308134.2:c.1581+1G>T	NP_001295063.1:n.1581+1G>T