Canonical Allele Identifier: CA2133607343

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159262C= , CM000676.2:g.45159262C=	GRCh38
NC_000014.8:g.45628465C= , CM000676.1:g.45628465C=	GRCh37
NC_000014.7:g.44698215C=	NCBI36
NG_007417.1:g.28330C= , LRG_502:g.28330C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1563C=	ENSP00000450596.1:p.Thr521=
ENST00000556250.6:c.1563C=	ENSP00000452033.2:p.Thr521=
ENST00000696641.1:c.1404C=	ENSP00000512774.1:p.Thr468=
ENST00000696642.1:c.*374C=	ENSP00000512775.1:n.*374C=
ENST00000696643.1:c.1563C=	ENSP00000512776.1:p.Thr521=
ENST00000696646.1:c.*374C=	ENSP00000512777.1:n.*374C=
ENST00000696647.1:c.1563C=	ENSP00000512778.1:p.Thr521=
ENST00000696648.1:c.1563C=	ENSP00000512779.1:p.Thr521=
ENST00000696649.1:c.1563C=	ENSP00000512780.1:p.Thr521=
ENST00000696650.1:n.1511C=
ENST00000696658.1:n.2113C=
ENST00000696662.1:c.1485C=	ENSP00000512788.1:p.Thr495=
ENST00000696663.1:c.380C=
ENST00000696664.1:c.380C=
ENST00000696675.1:c.1563C=	ENSP00000512799.1:p.Thr521=
ENST00000696680.1:c.1431C=	ENSP00000512803.1:p.Thr477=
ENST00000696681.1:c.*374C=	ENSP00000512804.1:n.*374C=
ENST00000696682.1:c.1563C=	ENSP00000512805.1:p.Thr521=
ENST00000696683.1:c.380C=
ENST00000696684.1:c.380C=
ENST00000696685.1:c.380C=
ENST00000267430.10:c.1563C= MANE Select	ENSP00000267430.5:p.Thr521=
ENST00000267430.9:c.1563C=	ENSP00000267430.5:p.Thr521=
ENST00000542564.6:c.1485C=	ENSP00000442493.2:p.Thr495=
ENST00000556036.5:c.1563C=	ENSP00000450596.1:p.Thr521=
ENST00000556250.5:c.318C=	ENSP00000452033.1:p.Thr106=
NM_001308133.1:c.1485C=	NP_001295062.1:p.Thr495=
NM_001308134.1:c.1563C=	NP_001295063.1:p.Thr521=
NM_020937.2:c.1563C= , LRG_502t1:c.1563C=	NP_065988.1:p.Thr521=
NM_020937.3:c.1563C=	NP_065988.1:p.Thr521=
XM_011537034.1:c.1563C=	XP_011535336.1:p.Thr521=
XM_011537035.1:c.1485C=	XP_011535337.1:p.Thr495=
XM_011537036.1:c.1563C=	XP_011535338.1:p.Thr521=
XM_011537034.2:c.1563C=	XP_011535336.1:p.Thr521=
XM_011537035.3:c.1485C=	XP_011535337.1:p.Thr495=
XM_017021523.1:c.1563C=	XP_016877012.1:p.Thr521=
XM_017021524.2:c.600C=	XP_016877013.1:p.Thr200=
XM_017021525.2:c.378C=	XP_016877014.1:p.Thr126=
XM_017021526.2:c.378C=	XP_016877015.1:p.Thr126=
XM_017021527.1:c.378C=	XP_016877016.1:p.Thr126=
XR_001750470.1:n.1655C=
XR_001750471.2:n.1655C=
XR_001750472.1:n.1655C=
NM_020937.4:c.1563C= MANE Select	NP_065988.1:p.Thr521=
NM_001308133.2:c.1485C=	NP_001295062.1:p.Thr495=
NM_001308134.2:c.1563C=	NP_001295063.1:p.Thr521=