Canonical Allele Identifier: CA2624699553

Gene: FANCM

Linked Data

• gnomAD v4: 14-45185211-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185212del , CM000676.2:g.45185212del	GRCh38
NC_000014.8:g.45654415del , CM000676.1:g.45654415del	GRCh37
NC_000014.7:g.44724165del	NCBI36
NG_007417.1:g.54280del , LRG_502:g.54280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2728-5del	ENSP00000450632.2:n.2728-5del
ENST00000555484.2:c.294-5del
ENST00000556250.6:c.4309-5del	ENSP00000452033.2:n.4309-5del
ENST00000557110.2:c.294-5del
ENST00000696642.1:c.*3327-5del	ENSP00000512775.1:n.*3327-5del
ENST00000696644.1:n.252-5del
ENST00000696645.1:n.406-5del
ENST00000696647.1:c.4516-5del	ENSP00000512778.1:n.4516-5del
ENST00000696648.1:c.*2541-5del	ENSP00000512779.1:n.*2541-5del
ENST00000696649.1:c.4360-5del	ENSP00000512780.1:n.4360-5del
ENST00000696650.1:n.4464-5del
ENST00000696659.1:c.2514-5del
ENST00000696663.1:c.3447-5del
ENST00000696664.1:c.3348-5del
ENST00000696665.1:c.294-5del
ENST00000696675.1:c.*272-5del	ENSP00000512799.1:n.*272-5del
ENST00000696683.1:c.3333-5del
ENST00000696684.1:c.3333-5del
ENST00000696685.1:c.3333-5del
ENST00000696686.1:n.1253-5del
ENST00000267430.10:c.4516-5del MANE Select	ENSP00000267430.5:n.4516-5del
ENST00000267430.9:c.4516-5del	ENSP00000267430.5:n.4516-5del
ENST00000542564.6:c.4438-5del	ENSP00000442493.2:n.4438-5del
ENST00000554809.5:c.1313-5del
ENST00000555013.1:n.349-5del
ENST00000556250.5:c.3064-5del	ENSP00000452033.1:n.3064-5del
NM_001308133.1:c.4438-5del	NP_001295062.1:n.4438-5del
NM_020937.2:c.4516-5del , LRG_502t1:c.4516-5del	NP_065988.1:n.4516-5del
NM_020937.3:c.4516-5del	NP_065988.1:n.4516-5del
XM_011537034.1:c.4531-5del	XP_011535336.1:n.4531-5del
XM_011537035.1:c.4453-5del	XP_011535337.1:n.4453-5del
XM_011537036.1:c.4531-5del	XP_011535338.1:n.4531-5del
XM_011537037.1:c.2545-5del	XP_011535339.1:n.2545-5del
XM_011537034.2:c.4531-5del	XP_011535336.1:n.4531-5del
XM_011537035.3:c.4453-5del	XP_011535337.1:n.4453-5del
XM_011537037.3:c.2545-5del	XP_011535339.1:n.2545-5del
XM_017021523.1:c.4531-5del	XP_016877012.1:n.4531-5del
XM_017021524.2:c.3568-5del	XP_016877013.1:n.3568-5del
XM_017021525.2:c.3346-5del	XP_016877014.1:n.3346-5del
XM_017021526.2:c.3346-5del	XP_016877015.1:n.3346-5del
XM_017021527.1:c.3331-5del	XP_016877016.1:n.3331-5del
XR_001750470.1:n.4623-5del
XR_001750471.2:n.4608-5del
XR_001750472.1:n.4660-5del
NM_020937.4:c.4516-5del MANE Select	NP_065988.1:n.4516-5del
NM_001308133.2:c.4438-5del	NP_001295062.1:n.4438-5del