Canonical Allele Identifier: CA7170070

Gene: FANCM

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45198718C>A , CM000676.2:g.45198718C>A	GRCh38
NC_000014.8:g.45667921C>A , CM000676.1:g.45667921C>A	GRCh37
NC_000014.7:g.44737671C>A	NCBI36
NG_007417.1:g.67786C>A , LRG_502:g.67786C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553551.2:n.1991C>A
ENST00000554809.6:c.4108C>A	ENSP00000450632.2:p.Arg1370=
ENST00000555484.2:c.1569C>A
ENST00000556250.6:c.5584C>A	ENSP00000452033.2:p.Arg1862=
ENST00000557110.2:c.1495-14C>A
ENST00000696645.1:n.1681C>A
ENST00000696647.1:c.*24C>A	ENSP00000512778.1:n.*24C>A
ENST00000696648.1:c.*3816C>A	ENSP00000512779.1:n.*3816C>A
ENST00000696649.1:c.5635C>A	ENSP00000512780.1:p.Arg1879=
ENST00000696651.1:n.2231C>A
ENST00000696659.1:c.3413C>A
ENST00000696663.1:c.4722C>A
ENST00000696664.1:c.4623C>A
ENST00000696665.1:c.1495-1152C>A
ENST00000696675.1:c.*1547C>A	ENSP00000512799.1:n.*1547C>A
ENST00000696683.1:c.4419C>A
ENST00000696684.1:c.4158-1152C>A
ENST00000696685.1:c.4609C>A
ENST00000696686.1:n.2528C>A
ENST00000267430.10:c.5791C>A MANE Select	ENSP00000267430.5:p.Arg1931=
ENST00000267430.9:c.5791C>A	ENSP00000267430.5:p.Arg1931=
ENST00000542564.6:c.5713C>A	ENSP00000442493.2:p.Arg1905=
ENST00000553551.1:n.284C>A
ENST00000554809.5:c.2693C>A
ENST00000555484.1:c.169C>A	ENSP00000450797.1:p.Arg57=
ENST00000556250.5:c.4339C>A	ENSP00000452033.1:p.Arg1447=
ENST00000557110.1:c.377-14C>A	ENSP00000451846.1:n.377-14C>A
NM_001308133.1:c.5713C>A	NP_001295062.1:p.Arg1905=
NM_020937.2:c.5791C>A , LRG_502t1:c.5791C>A	NP_065988.1:p.Arg1931=
NM_020937.3:c.5791C>A	NP_065988.1:p.Arg1931=
XM_011537034.1:c.5806C>A	XP_011535336.1:p.Arg1936=
XM_011537035.1:c.5728C>A	XP_011535337.1:p.Arg1910=
XM_011537036.1:c.*24C>A	XP_011535338.1:n.*24C>A
XM_011537037.1:c.3820C>A	XP_011535339.1:p.Arg1274=
XM_011537034.2:c.5806C>A	XP_011535336.1:p.Arg1936=
XM_011537035.3:c.5728C>A	XP_011535337.1:p.Arg1910=
XM_011537037.3:c.3820C>A	XP_011535339.1:p.Arg1274=
XM_017021523.1:c.5356-1152C>A	XP_016877012.1:n.5356-1152C>A
XM_017021524.2:c.4843C>A	XP_016877013.1:p.Arg1615=
XM_017021525.2:c.4621C>A	XP_016877014.1:p.Arg1541=
XM_017021526.2:c.4621C>A	XP_016877015.1:p.Arg1541=
XM_017021527.1:c.4606C>A	XP_016877016.1:p.Arg1536=
XR_001750470.1:n.5522C>A
XR_001750471.2:n.5507C>A
NM_020937.4:c.5791C>A MANE Select	NP_065988.1:p.Arg1931=
NM_001308133.2:c.5713C>A	NP_001295062.1:p.Arg1905=