Canonical Allele Identifier: CA2624698271

Gene: FANCM

Linked Data

• gnomAD v4: 14-45166822-CTAAGTATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45166828_45166835del , CM000676.2:g.45166828_45166835del	GRCh38
NC_000014.8:g.45636031_45636038del , CM000676.1:g.45636031_45636038del	GRCh37
NC_000014.7:g.44705781_44705788del	NCBI36
NG_007417.1:g.35896_35903del , LRG_502:g.35896_35903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1789-122_1789-115del	ENSP00000450596.1:n.1789-122_1789-115del
ENST00000556250.6:c.1582-122_1582-115del	ENSP00000452033.2:n.1582-122_1582-115del
ENST00000696641.1:c.1630-122_1630-115del	ENSP00000512774.1:n.1630-122_1630-115del
ENST00000696642.1:c.*600-122_*600-115del	ENSP00000512775.1:n.*600-122_*600-115del
ENST00000696646.1:c.*600-122_*600-115del	ENSP00000512777.1:n.*600-122_*600-115del
ENST00000696647.1:c.1789-122_1789-115del	ENSP00000512778.1:n.1789-122_1789-115del
ENST00000696648.1:c.1789-122_1789-115del	ENSP00000512779.1:n.1789-122_1789-115del
ENST00000696649.1:c.1789-122_1789-115del	ENSP00000512780.1:n.1789-122_1789-115del
ENST00000696650.1:n.1737-122_1737-115del
ENST00000696658.1:n.2339-122_2339-115del
ENST00000696662.1:c.1711-122_1711-115del	ENSP00000512788.1:n.1711-122_1711-115del
ENST00000696663.1:c.606-122_606-115del
ENST00000696664.1:c.606-122_606-115del
ENST00000696675.1:c.1789-122_1789-115del	ENSP00000512799.1:n.1789-122_1789-115del
ENST00000696683.1:c.606-122_606-115del
ENST00000696684.1:c.606-122_606-115del
ENST00000696685.1:c.606-122_606-115del
ENST00000267430.10:c.1789-122_1789-115del MANE Select	ENSP00000267430.5:n.1789-122_1789-115del
ENST00000267430.9:c.1789-122_1789-115del	ENSP00000267430.5:n.1789-122_1789-115del
ENST00000542564.6:c.1711-122_1711-115del	ENSP00000442493.2:n.1711-122_1711-115del
ENST00000556036.5:c.1789-122_1789-115del	ENSP00000450596.1:n.1789-122_1789-115del
ENST00000556250.5:c.337-122_337-115del	ENSP00000452033.1:n.337-122_337-115del
NM_001308133.1:c.1711-122_1711-115del	NP_001295062.1:n.1711-122_1711-115del
NM_001308134.1:c.1789-122_1789-115del	NP_001295063.1:n.1789-122_1789-115del
NM_020937.2:c.1789-122_1789-115del , LRG_502t1:c.1789-122_1789-115del	NP_065988.1:n.1789-122_1789-115del
NM_020937.3:c.1789-122_1789-115del	NP_065988.1:n.1789-122_1789-115del
XM_011537034.1:c.1789-122_1789-115del	XP_011535336.1:n.1789-122_1789-115del
XM_011537035.1:c.1711-122_1711-115del	XP_011535337.1:n.1711-122_1711-115del
XM_011537036.1:c.1789-122_1789-115del	XP_011535338.1:n.1789-122_1789-115del
XM_011537034.2:c.1789-122_1789-115del	XP_011535336.1:n.1789-122_1789-115del
XM_011537035.3:c.1711-122_1711-115del	XP_011535337.1:n.1711-122_1711-115del
XM_017021523.1:c.1789-122_1789-115del	XP_016877012.1:n.1789-122_1789-115del
XM_017021524.2:c.826-122_826-115del	XP_016877013.1:n.826-122_826-115del
XM_017021525.2:c.604-122_604-115del	XP_016877014.1:n.604-122_604-115del
XM_017021526.2:c.604-122_604-115del	XP_016877015.1:n.604-122_604-115del
XM_017021527.1:c.604-122_604-115del	XP_016877016.1:n.604-122_604-115del
XR_001750470.1:n.1881-122_1881-115del
XR_001750471.2:n.1881-122_1881-115del
XR_001750472.1:n.1881-122_1881-115del
NM_020937.4:c.1789-122_1789-115del MANE Select	NP_065988.1:n.1789-122_1789-115del
NM_001308133.2:c.1711-122_1711-115del	NP_001295062.1:n.1711-122_1711-115del
NM_001308134.2:c.1789-122_1789-115del	NP_001295063.1:n.1789-122_1789-115del