Canonical Allele Identifier: CA486138407

Gene: FANCM

Linked Data

• ClinVar Variation Id: 2031976
• ClinVar RCV Id: RCV002876640
• MyVariant Identifiers: chr14:g.45623901G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154698G>T , CM000676.2:g.45154698G>T	GRCh38
NC_000014.8:g.45623901G>T , CM000676.1:g.45623901G>T	GRCh37
NC_000014.7:g.44693651G>T	NCBI36
NG_007417.1:g.23766G>T , LRG_502:g.23766G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000556036.6:c.1185G>T	ENSP00000450596.1:p.Gly395=
ENST00000556250.6:c.1185G>T	ENSP00000452033.2:p.Gly395=
ENST00000696641.1:c.1026G>T	ENSP00000512774.1:p.Gly342=
ENST00000696642.1:c.1052G>T	ENSP00000512775.1:p.Gly351Val
ENST00000696643.1:c.1185G>T	ENSP00000512776.1:p.Gly395=
ENST00000696646.1:c.974G>T	ENSP00000512777.1:p.Gly325Val
ENST00000696647.1:c.1185G>T	ENSP00000512778.1:p.Gly395=
ENST00000696648.1:c.1185G>T	ENSP00000512779.1:p.Gly395=
ENST00000696649.1:c.1185G>T	ENSP00000512780.1:p.Gly395=
ENST00000696650.1:n.1133G>T
ENST00000696657.1:c.*403G>T	ENSP00000512784.1:n.*403G>T
ENST00000696658.1:n.1735G>T
ENST00000696662.1:c.1107G>T	ENSP00000512788.1:p.Gly369=
ENST00000696663.1:c.2G>T
ENST00000696664.1:c.2G>T
ENST00000696675.1:c.1185G>T	ENSP00000512799.1:p.Gly395=
ENST00000696680.1:c.1053G>T	ENSP00000512803.1:p.Gly351=
ENST00000696681.1:c.1052G>T	ENSP00000512804.1:p.Gly351Val
ENST00000696682.1:c.1185G>T	ENSP00000512805.1:p.Gly395=
ENST00000696683.1:c.2G>T
ENST00000696684.1:c.2G>T
ENST00000696685.1:c.2G>T
ENST00000267430.10:c.1185G>T MANE Select	ENSP00000267430.5:p.Gly395=
ENST00000267430.9:c.1185G>T	ENSP00000267430.5:p.Gly395=
ENST00000542564.6:c.1107G>T	ENSP00000442493.2:p.Gly369=
ENST00000556036.5:c.1185G>T	ENSP00000450596.1:p.Gly395=
NM_001308133.1:c.1107G>T	NP_001295062.1:p.Gly369=
NM_001308134.1:c.1185G>T	NP_001295063.1:p.Gly395=
NM_020937.2:c.1185G>T , LRG_502t1:c.1185G>T	NP_065988.1:p.Gly395=
NM_020937.3:c.1185G>T	NP_065988.1:p.Gly395=
XM_011537034.1:c.1185G>T	XP_011535336.1:p.Gly395=
XM_011537035.1:c.1107G>T	XP_011535337.1:p.Gly369=
XM_011537036.1:c.1185G>T	XP_011535338.1:p.Gly395=
XM_011537034.2:c.1185G>T	XP_011535336.1:p.Gly395=
XM_011537035.3:c.1107G>T	XP_011535337.1:p.Gly369=
XM_017021523.1:c.1185G>T	XP_016877012.1:p.Gly395=
XM_017021524.2:c.222G>T	XP_016877013.1:p.Gly74=
XM_017021525.2:c.-1G>T	XP_016877014.1:n.-1G>T
XM_017021526.2:c.-1G>T	XP_016877015.1:n.-1G>T
XM_017021527.1:c.-1G>T	XP_016877016.1:n.-1G>T
XR_001750470.1:n.1277G>T
XR_001750471.2:n.1277G>T
XR_001750472.1:n.1277G>T
NM_020937.4:c.1185G>T MANE Select	NP_065988.1:p.Gly395=
NM_001308133.2:c.1107G>T	NP_001295062.1:p.Gly369=
NM_001308134.2:c.1185G>T	NP_001295063.1:p.Gly395=