Canonical Allele Identifier: CA2624697640

Gene: FANCM

Linked Data

• gnomAD v4: 14-45154770-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154773del , CM000676.2:g.45154773del	GRCh38
NC_000014.8:g.45623976del , CM000676.1:g.45623976del	GRCh37
NC_000014.7:g.44693726del	NCBI36
NG_007417.1:g.23841del , LRG_502:g.23841del

Transcript Alleles

HGVS	Amino-acid change
ENST00000556036.6:c.1260del	ENSP00000450596.1:p.Phe420LeufsTer?
ENST00000556250.6:c.1260del	ENSP00000452033.2:p.Phe420LeufsTer?
ENST00000696641.1:c.1101del	ENSP00000512774.1:p.Phe367LeufsTer?
ENST00000696642.1:c.*71del	ENSP00000512775.1:n.*71del
ENST00000696643.1:c.1260del	ENSP00000512776.1:p.Phe420LeufsTer?
ENST00000696646.1:c.*71del	ENSP00000512777.1:n.*71del
ENST00000696647.1:c.1260del	ENSP00000512778.1:p.Phe420LeufsTer?
ENST00000696648.1:c.1260del	ENSP00000512779.1:p.Phe420LeufsTer?
ENST00000696649.1:c.1260del	ENSP00000512780.1:p.Phe420LeufsTer?
ENST00000696650.1:n.1208del
ENST00000696657.1:c.*478del	ENSP00000512784.1:n.*478del
ENST00000696658.1:n.1810del
ENST00000696662.1:c.1182del	ENSP00000512788.1:p.Phe394LeufsTer?
ENST00000696663.1:c.77del
ENST00000696664.1:c.77del
ENST00000696675.1:c.1260del	ENSP00000512799.1:p.Phe420LeufsTer?
ENST00000696680.1:c.1128del	ENSP00000512803.1:p.Phe376LeufsTer?
ENST00000696681.1:c.*71del	ENSP00000512804.1:n.*71del
ENST00000696682.1:c.1260del	ENSP00000512805.1:p.Phe420LeufsTer?
ENST00000696683.1:c.77del
ENST00000696684.1:c.77del
ENST00000696685.1:c.77del
ENST00000267430.10:c.1260del MANE Select	ENSP00000267430.5:p.Phe420LeufsTer?
ENST00000267430.9:c.1260del	ENSP00000267430.5:p.Phe420LeufsTer?
ENST00000542564.6:c.1182del	ENSP00000442493.2:p.Phe394LeufsTer?
ENST00000556036.5:c.1260del	ENSP00000450596.1:p.Phe420LeufsTer?
ENST00000556250.5:c.15del	ENSP00000452033.1:p.Phe5LeufsTer?
NM_001308133.1:c.1182del	NP_001295062.1:p.Phe394LeufsTer?
NM_001308134.1:c.1260del	NP_001295063.1:p.Phe420LeufsTer?
NM_020937.2:c.1260del , LRG_502t1:c.1260del	NP_065988.1:p.Phe420LeufsTer?
NM_020937.3:c.1260del	NP_065988.1:p.Phe420LeufsTer?
XM_011537034.1:c.1260del	XP_011535336.1:p.Phe420LeufsTer?
XM_011537035.1:c.1182del	XP_011535337.1:p.Phe394LeufsTer?
XM_011537036.1:c.1260del	XP_011535338.1:p.Phe420LeufsTer?
XM_011537034.2:c.1260del	XP_011535336.1:p.Phe420LeufsTer?
XM_011537035.3:c.1182del	XP_011535337.1:p.Phe394LeufsTer?
XM_017021523.1:c.1260del	XP_016877012.1:p.Phe420LeufsTer?
XM_017021524.2:c.297del	XP_016877013.1:p.Phe99LeufsTer?
XM_017021525.2:c.75del	XP_016877014.1:p.Phe25LeufsTer?
XM_017021526.2:c.75del	XP_016877015.1:p.Phe25LeufsTer?
XM_017021527.1:c.75del	XP_016877016.1:p.Phe25LeufsTer?
XR_001750470.1:n.1352del
XR_001750471.2:n.1352del
XR_001750472.1:n.1352del
NM_020937.4:c.1260del MANE Select	NP_065988.1:p.Phe420LeufsTer?
NM_001308133.2:c.1182del	NP_001295062.1:p.Phe394LeufsTer?
NM_001308134.2:c.1260del	NP_001295063.1:p.Phe420LeufsTer?