Canonical Allele Identifier: CA389601900

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45176277C>T , CM000676.2:g.45176277C>T	GRCh38
NC_000014.8:g.45645480C>T , CM000676.1:g.45645480C>T	GRCh37
NC_000014.7:g.44715230C>T	NCBI36
NG_007417.1:g.45345C>T , LRG_502:g.45345C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.3523C>T MANE Select	NP_065988.1:p.Gln1175Ter
ENST00000267430.10:c.3523C>T MANE Select	ENSP00000267430.5:p.Gln1175Ter
NM_001308133.1:c.3445C>T	NP_001295062.1:p.Gln1149Ter
NM_001308133.2:c.3445C>T	NP_001295062.1:p.Gln1149Ter
NM_020937.2:c.3523C>T , LRG_502t1:c.3523C>T	NP_065988.1:p.Gln1175Ter
NM_020937.3:c.3523C>T	NP_065988.1:p.Gln1175Ter
ENST00000267430.9:c.3523C>T	ENSP00000267430.5:p.Gln1175Ter
ENST00000542564.6:c.3445C>T	ENSP00000442493.2:p.Gln1149Ter
ENST00000554809.5:c.320C>T
ENST00000554809.6:c.1735C>T	ENSP00000450632.2:p.Gln579Ter
ENST00000556250.5:c.2071C>T	ENSP00000452033.1:p.Gln691Ter
ENST00000556250.6:c.3316C>T	ENSP00000452033.2:p.Gln1106Ter
ENST00000696641.1:c.3364C>T	ENSP00000512774.1:p.Gln1122Ter
ENST00000696642.1:c.*2334C>T	ENSP00000512775.1:n.*2334C>T
ENST00000696646.1:c.*2334C>T	ENSP00000512777.1:n.*2334C>T
ENST00000696647.1:c.3523C>T	ENSP00000512778.1:p.Gln1175Ter
ENST00000696648.1:c.*1548C>T	ENSP00000512779.1:n.*1548C>T
ENST00000696649.1:c.3367C>T	ENSP00000512780.1:p.Gln1123Ter
ENST00000696650.1:n.3471C>T
ENST00000696659.1:c.1521C>T
ENST00000696663.1:c.2340C>T
ENST00000696664.1:c.2340C>T
ENST00000696675.1:c.3523C>T	ENSP00000512799.1:p.Gln1175Ter
ENST00000696683.1:c.2340C>T
ENST00000696684.1:c.2340C>T
ENST00000696685.1:c.2340C>T
XM_011537034.1:c.3523C>T	XP_011535336.1:p.Gln1175Ter
XM_011537034.2:c.3523C>T	XP_011535336.1:p.Gln1175Ter
XM_011537035.1:c.3445C>T	XP_011535337.1:p.Gln1149Ter
XM_011537035.3:c.3445C>T	XP_011535337.1:p.Gln1149Ter
XM_011537036.1:c.3523C>T	XP_011535338.1:p.Gln1175Ter
XM_011537037.1:c.1537C>T	XP_011535339.1:p.Gln513Ter
XM_011537037.3:c.1537C>T	XP_011535339.1:p.Gln513Ter
XM_017021523.1:c.3523C>T	XP_016877012.1:p.Gln1175Ter
XM_017021524.2:c.2560C>T	XP_016877013.1:p.Gln854Ter
XM_017021525.2:c.2338C>T	XP_016877014.1:p.Gln780Ter
XM_017021526.2:c.2338C>T	XP_016877015.1:p.Gln780Ter
XM_017021527.1:c.2338C>T	XP_016877016.1:p.Gln780Ter
XR_001750470.1:n.3615C>T
XR_001750471.2:n.3615C>T
XR_001750472.1:n.3615C>T