Canonical Allele Identifier: CA2133624506

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185279T= , CM000676.2:g.45185279T=	GRCh38
NC_000014.8:g.45654482T= , CM000676.1:g.45654482T=	GRCh37
NC_000014.7:g.44724232T=	NCBI36
NG_007417.1:g.54347T= , LRG_502:g.54347T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2790T=	ENSP00000450632.2:p.Val930=
ENST00000555484.2:c.356T=
ENST00000556250.6:c.4371T=	ENSP00000452033.2:p.Val1457=
ENST00000557110.2:c.356T=
ENST00000696642.1:c.*3389T=	ENSP00000512775.1:n.*3389T=
ENST00000696644.1:n.314T=
ENST00000696645.1:n.468T=
ENST00000696647.1:c.4578T=	ENSP00000512778.1:p.Val1526=
ENST00000696648.1:c.*2603T=	ENSP00000512779.1:n.*2603T=
ENST00000696649.1:c.4422T=	ENSP00000512780.1:p.Val1474=
ENST00000696650.1:n.4526T=
ENST00000696659.1:c.2576T=
ENST00000696663.1:c.3509T=
ENST00000696664.1:c.3410T=
ENST00000696665.1:c.356T=
ENST00000696675.1:c.*334T=	ENSP00000512799.1:n.*334T=
ENST00000696683.1:c.3395T=
ENST00000696684.1:c.3395T=
ENST00000696685.1:c.3395T=
ENST00000696686.1:n.1315T=
ENST00000267430.10:c.4578T= MANE Select	ENSP00000267430.5:p.Val1526=
ENST00000267430.9:c.4578T=	ENSP00000267430.5:p.Val1526=
ENST00000542564.6:c.4500T=	ENSP00000442493.2:p.Val1500=
ENST00000554809.5:c.1375T=
ENST00000555013.1:n.411T=
ENST00000556250.5:c.3126T=	ENSP00000452033.1:p.Val1042=
NM_001308133.1:c.4500T=	NP_001295062.1:p.Val1500=
NM_020937.2:c.4578T= , LRG_502t1:c.4578T=	NP_065988.1:p.Val1526=
NM_020937.3:c.4578T=	NP_065988.1:p.Val1526=
XM_011537034.1:c.4593T=	XP_011535336.1:p.Val1531=
XM_011537035.1:c.4515T=	XP_011535337.1:p.Val1505=
XM_011537036.1:c.4593T=	XP_011535338.1:p.Val1531=
XM_011537037.1:c.2607T=	XP_011535339.1:p.Val869=
XM_011537034.2:c.4593T=	XP_011535336.1:p.Val1531=
XM_011537035.3:c.4515T=	XP_011535337.1:p.Val1505=
XM_011537037.3:c.2607T=	XP_011535339.1:p.Val869=
XM_017021523.1:c.4593T=	XP_016877012.1:p.Val1531=
XM_017021524.2:c.3630T=	XP_016877013.1:p.Val1210=
XM_017021525.2:c.3408T=	XP_016877014.1:p.Val1136=
XM_017021526.2:c.3408T=	XP_016877015.1:p.Val1136=
XM_017021527.1:c.3393T=	XP_016877016.1:p.Val1131=
XR_001750470.1:n.4685T=
XR_001750471.2:n.4670T=
XR_001750472.1:n.4722T=
NM_020937.4:c.4578T= MANE Select	NP_065988.1:p.Val1526=
NM_001308133.2:c.4500T=	NP_001295062.1:p.Val1500=