Canonical Allele Identifier: CA2624697594

Gene: FANCM

Linked Data

• gnomAD v4: 14-45154661-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45154663del , CM000676.2:g.45154663del	GRCh38
NC_000014.8:g.45623866del , CM000676.1:g.45623866del	GRCh37
NC_000014.7:g.44693616del	NCBI36
NG_007417.1:g.23731del , LRG_502:g.23731del

Transcript Alleles

HGVS	Amino-acid change
ENST00000556036.6:c.1184-34del	ENSP00000450596.1:n.1184-34del
ENST00000556250.6:c.1184-34del	ENSP00000452033.2:n.1184-34del
ENST00000696641.1:c.1025-34del	ENSP00000512774.1:n.1025-34del
ENST00000696642.1:c.1051-34del	ENSP00000512775.1:n.1051-34del
ENST00000696643.1:c.1184-34del	ENSP00000512776.1:n.1184-34del
ENST00000696646.1:c.973-34del	ENSP00000512777.1:n.973-34del
ENST00000696647.1:c.1184-34del	ENSP00000512778.1:n.1184-34del
ENST00000696648.1:c.1184-34del	ENSP00000512779.1:n.1184-34del
ENST00000696649.1:c.1184-34del	ENSP00000512780.1:n.1184-34del
ENST00000696650.1:n.1132-34del
ENST00000696657.1:c.*402-34del	ENSP00000512784.1:n.*402-34del
ENST00000696658.1:n.1734-34del
ENST00000696662.1:c.1106-34del	ENSP00000512788.1:n.1106-34del
ENST00000696675.1:c.1184-34del	ENSP00000512799.1:n.1184-34del
ENST00000696680.1:c.1052-34del	ENSP00000512803.1:n.1052-34del
ENST00000696681.1:c.1051-34del	ENSP00000512804.1:n.1051-34del
ENST00000696682.1:c.1184-34del	ENSP00000512805.1:n.1184-34del
ENST00000267430.10:c.1184-34del MANE Select	ENSP00000267430.5:n.1184-34del
ENST00000267430.9:c.1184-34del	ENSP00000267430.5:n.1184-34del
ENST00000542564.6:c.1106-34del	ENSP00000442493.2:n.1106-34del
ENST00000556036.5:c.1184-34del	ENSP00000450596.1:n.1184-34del
NM_001308133.1:c.1106-34del	NP_001295062.1:n.1106-34del
NM_001308134.1:c.1184-34del	NP_001295063.1:n.1184-34del
NM_020937.2:c.1184-34del , LRG_502t1:c.1184-34del	NP_065988.1:n.1184-34del
NM_020937.3:c.1184-34del	NP_065988.1:n.1184-34del
XM_011537034.1:c.1184-34del	XP_011535336.1:n.1184-34del
XM_011537035.1:c.1106-34del	XP_011535337.1:n.1106-34del
XM_011537036.1:c.1184-34del	XP_011535338.1:n.1184-34del
XM_011537034.2:c.1184-34del	XP_011535336.1:n.1184-34del
XM_011537035.3:c.1106-34del	XP_011535337.1:n.1106-34del
XM_017021523.1:c.1184-34del	XP_016877012.1:n.1184-34del
XM_017021524.2:c.221-34del	XP_016877013.1:n.221-34del
XM_017021525.2:c.-2-34del	XP_016877014.1:n.-2-34del
XM_017021526.2:c.-2-34del	XP_016877015.1:n.-2-34del
XM_017021527.1:c.-2-34del	XP_016877016.1:n.-2-34del
XR_001750470.1:n.1276-34del
XR_001750471.2:n.1276-34del
XR_001750472.1:n.1276-34del
NM_020937.4:c.1184-34del MANE Select	NP_065988.1:n.1184-34del
NM_001308133.2:c.1106-34del	NP_001295062.1:n.1106-34del
NM_001308134.2:c.1184-34del	NP_001295063.1:n.1184-34del