Canonical Allele Identifier: CA2575516371

Gene: FANCM

Linked Data

• gnomAD v4: 14-45185182-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185182T>G , CM000676.2:g.45185182T>G	GRCh38
NC_000014.8:g.45654385T>G , CM000676.1:g.45654385T>G	GRCh37
NC_000014.7:g.44724135T>G	NCBI36
NG_007417.1:g.54250T>G , LRG_502:g.54250T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2728-35T>G	ENSP00000450632.2:n.2728-35T>G
ENST00000555484.2:c.294-35T>G
ENST00000556250.6:c.4309-35T>G	ENSP00000452033.2:n.4309-35T>G
ENST00000557110.2:c.294-35T>G
ENST00000696642.1:c.*3327-35T>G	ENSP00000512775.1:n.*3327-35T>G
ENST00000696644.1:n.252-35T>G
ENST00000696645.1:n.406-35T>G
ENST00000696647.1:c.4516-35T>G	ENSP00000512778.1:n.4516-35T>G
ENST00000696648.1:c.*2541-35T>G	ENSP00000512779.1:n.*2541-35T>G
ENST00000696649.1:c.4360-35T>G	ENSP00000512780.1:n.4360-35T>G
ENST00000696650.1:n.4464-35T>G
ENST00000696659.1:c.2514-35T>G
ENST00000696663.1:c.3447-35T>G
ENST00000696664.1:c.3348-35T>G
ENST00000696665.1:c.294-35T>G
ENST00000696675.1:c.*272-35T>G	ENSP00000512799.1:n.*272-35T>G
ENST00000696683.1:c.3333-35T>G
ENST00000696684.1:c.3333-35T>G
ENST00000696685.1:c.3333-35T>G
ENST00000696686.1:n.1253-35T>G
ENST00000267430.10:c.4516-35T>G MANE Select	ENSP00000267430.5:n.4516-35T>G
ENST00000267430.9:c.4516-35T>G	ENSP00000267430.5:n.4516-35T>G
ENST00000542564.6:c.4438-35T>G	ENSP00000442493.2:n.4438-35T>G
ENST00000554809.5:c.1313-35T>G
ENST00000555013.1:n.349-35T>G
ENST00000556250.5:c.3064-35T>G	ENSP00000452033.1:n.3064-35T>G
NM_001308133.1:c.4438-35T>G	NP_001295062.1:n.4438-35T>G
NM_020937.2:c.4516-35T>G , LRG_502t1:c.4516-35T>G	NP_065988.1:n.4516-35T>G
NM_020937.3:c.4516-35T>G	NP_065988.1:n.4516-35T>G
XM_011537034.1:c.4531-35T>G	XP_011535336.1:n.4531-35T>G
XM_011537035.1:c.4453-35T>G	XP_011535337.1:n.4453-35T>G
XM_011537036.1:c.4531-35T>G	XP_011535338.1:n.4531-35T>G
XM_011537037.1:c.2545-35T>G	XP_011535339.1:n.2545-35T>G
XM_011537034.2:c.4531-35T>G	XP_011535336.1:n.4531-35T>G
XM_011537035.3:c.4453-35T>G	XP_011535337.1:n.4453-35T>G
XM_011537037.3:c.2545-35T>G	XP_011535339.1:n.2545-35T>G
XM_017021523.1:c.4531-35T>G	XP_016877012.1:n.4531-35T>G
XM_017021524.2:c.3568-35T>G	XP_016877013.1:n.3568-35T>G
XM_017021525.2:c.3346-35T>G	XP_016877014.1:n.3346-35T>G
XM_017021526.2:c.3346-35T>G	XP_016877015.1:n.3346-35T>G
XM_017021527.1:c.3331-35T>G	XP_016877016.1:n.3331-35T>G
XR_001750470.1:n.4623-35T>G
XR_001750471.2:n.4608-35T>G
XR_001750472.1:n.4660-35T>G
NM_020937.4:c.4516-35T>G MANE Select	NP_065988.1:n.4516-35T>G
NM_001308133.2:c.4438-35T>G	NP_001295062.1:n.4438-35T>G