Canonical Allele Identifier: CA2133607406

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159299_45159305delinsGATAAAA , CM000676.2:g.45159299_45159305delinsGATAAAA	GRCh38
NC_000014.8:g.45628502_45628508delinsGATAAAA , CM000676.1:g.45628502_45628508delinsGATAAAA	GRCh37
NC_000014.7:g.44698252_44698258delinsGATAAAA	NCBI36
NG_007417.1:g.28367_28373delinsGATAAAA , LRG_502:g.28367_28373delinsGATAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1581+19_1581+25delinsGATAAAA	ENSP00000450596.1:n.1581+19_1581+25delinsGATAAAA
ENST00000556250.6:c.1581+19_1581+25delinsGATAAAA	ENSP00000452033.2:n.1581+19_1581+25delinsGATAAAA
ENST00000696641.1:c.1422+19_1422+25delinsGATAAAA	ENSP00000512774.1:n.1422+19_1422+25delinsGATAAAA
ENST00000696642.1:c.*392+19_*392+25delinsGATAAAA	ENSP00000512775.1:n.*392+19_*392+25delinsGATAAAA
ENST00000696643.1:c.1600_1606delinsGATAAAA	ENSP00000512776.1:p.Asp534=
ENST00000696646.1:c.*392+19_*392+25delinsGATAAAA	ENSP00000512777.1:n.*392+19_*392+25delinsGATAAAA
ENST00000696647.1:c.1581+19_1581+25delinsGATAAAA	ENSP00000512778.1:n.1581+19_1581+25delinsGATAAAA
ENST00000696648.1:c.1581+19_1581+25delinsGATAAAA	ENSP00000512779.1:n.1581+19_1581+25delinsGATAAAA
ENST00000696649.1:c.1581+19_1581+25delinsGATAAAA	ENSP00000512780.1:n.1581+19_1581+25delinsGATAAAA
ENST00000696650.1:n.1529+19_1529+25delinsGATAAAA
ENST00000696658.1:n.2131+19_2131+25delinsGATAAAA
ENST00000696662.1:c.1503+19_1503+25delinsGATAAAA	ENSP00000512788.1:n.1503+19_1503+25delinsGATAAAA
ENST00000696663.1:c.398+19_398+25delinsGATAAAA
ENST00000696664.1:c.398+19_398+25delinsGATAAAA
ENST00000696675.1:c.1581+19_1581+25delinsGATAAAA	ENSP00000512799.1:n.1581+19_1581+25delinsGATAAAA
ENST00000696681.1:c.*411_*417delinsGATAAAA	ENSP00000512804.1:n.*411_*417delinsGATAAAA
ENST00000696682.1:c.1581+19_1581+25delinsGATAAAA	ENSP00000512805.1:n.1581+19_1581+25delinsGATAAAA
ENST00000696683.1:c.398+19_398+25delinsGATAAAA
ENST00000696684.1:c.398+19_398+25delinsGATAAAA
ENST00000696685.1:c.398+19_398+25delinsGATAAAA
ENST00000267430.10:c.1581+19_1581+25delinsGATAAAA MANE Select	ENSP00000267430.5:n.1581+19_1581+25delinsGATAAAA
ENST00000267430.9:c.1581+19_1581+25delinsGATAAAA	ENSP00000267430.5:n.1581+19_1581+25delinsGATAAAA
ENST00000542564.6:c.1503+19_1503+25delinsGATAAAA	ENSP00000442493.2:n.1503+19_1503+25delinsGATAAAA
ENST00000556036.5:c.1581+19_1581+25delinsGATAAAA	ENSP00000450596.1:n.1581+19_1581+25delinsGATAAAA
ENST00000556250.5:c.336+19_336+25delinsGATAAAA	ENSP00000452033.1:n.336+19_336+25delinsGATAAAA
NM_001308133.1:c.1503+19_1503+25delinsGATAAAA	NP_001295062.1:n.1503+19_1503+25delinsGATAAAA
NM_001308134.1:c.1581+19_1581+25delinsGATAAAA	NP_001295063.1:n.1581+19_1581+25delinsGATAAAA
NM_020937.2:c.1581+19_1581+25delinsGATAAAA , LRG_502t1:c.1581+19_1581+25delinsGATAAAA	NP_065988.1:n.1581+19_1581+25delinsGATAAAA
NM_020937.3:c.1581+19_1581+25delinsGATAAAA	NP_065988.1:n.1581+19_1581+25delinsGATAAAA
XM_011537034.1:c.1581+19_1581+25delinsGATAAAA	XP_011535336.1:n.1581+19_1581+25delinsGATAAAA
XM_011537035.1:c.1503+19_1503+25delinsGATAAAA	XP_011535337.1:n.1503+19_1503+25delinsGATAAAA
XM_011537036.1:c.1581+19_1581+25delinsGATAAAA	XP_011535338.1:n.1581+19_1581+25delinsGATAAAA
XM_011537034.2:c.1581+19_1581+25delinsGATAAAA	XP_011535336.1:n.1581+19_1581+25delinsGATAAAA
XM_011537035.3:c.1503+19_1503+25delinsGATAAAA	XP_011535337.1:n.1503+19_1503+25delinsGATAAAA
XM_017021523.1:c.1581+19_1581+25delinsGATAAAA	XP_016877012.1:n.1581+19_1581+25delinsGATAAAA
XM_017021524.2:c.618+19_618+25delinsGATAAAA	XP_016877013.1:n.618+19_618+25delinsGATAAAA
XM_017021525.2:c.396+19_396+25delinsGATAAAA	XP_016877014.1:n.396+19_396+25delinsGATAAAA
XM_017021526.2:c.396+19_396+25delinsGATAAAA	XP_016877015.1:n.396+19_396+25delinsGATAAAA
XM_017021527.1:c.396+19_396+25delinsGATAAAA	XP_016877016.1:n.396+19_396+25delinsGATAAAA
XR_001750470.1:n.1673+19_1673+25delinsGATAAAA
XR_001750471.2:n.1673+19_1673+25delinsGATAAAA
XR_001750472.1:n.1673+19_1673+25delinsGATAAAA
NM_020937.4:c.1581+19_1581+25delinsGATAAAA MANE Select	NP_065988.1:n.1581+19_1581+25delinsGATAAAA
NM_001308133.2:c.1503+19_1503+25delinsGATAAAA	NP_001295062.1:n.1503+19_1503+25delinsGATAAAA
NM_001308134.2:c.1581+19_1581+25delinsGATAAAA	NP_001295063.1:n.1581+19_1581+25delinsGATAAAA