Canonical Allele Identifier: CA2624699524

Gene: FANCM

Linked Data

• gnomAD v4: 14-45185184-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185185_45185186insCT , CM000676.2:g.45185185_45185186insCT	GRCh38
NC_000014.8:g.45654388_45654389insCT , CM000676.1:g.45654388_45654389insCT	GRCh37
NC_000014.7:g.44724138_44724139insCT	NCBI36
NG_007417.1:g.54253_54254insCT , LRG_502:g.54253_54254insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2728-32_2728-31insCT	ENSP00000450632.2:n.2728-32_2728-31insCT
ENST00000555484.2:c.294-32_294-31insCT
ENST00000556250.6:c.4309-32_4309-31insCT	ENSP00000452033.2:n.4309-32_4309-31insCT
ENST00000557110.2:c.294-32_294-31insCT
ENST00000696642.1:c.*3327-32_*3327-31insCT	ENSP00000512775.1:n.*3327-32_*3327-31insCT
ENST00000696644.1:n.252-32_252-31insCT
ENST00000696645.1:n.406-32_406-31insCT
ENST00000696647.1:c.4516-32_4516-31insCT	ENSP00000512778.1:n.4516-32_4516-31insCT
ENST00000696648.1:c.*2541-32_*2541-31insCT	ENSP00000512779.1:n.*2541-32_*2541-31insCT
ENST00000696649.1:c.4360-32_4360-31insCT	ENSP00000512780.1:n.4360-32_4360-31insCT
ENST00000696650.1:n.4464-32_4464-31insCT
ENST00000696659.1:c.2514-32_2514-31insCT
ENST00000696663.1:c.3447-32_3447-31insCT
ENST00000696664.1:c.3348-32_3348-31insCT
ENST00000696665.1:c.294-32_294-31insCT
ENST00000696675.1:c.*272-32_*272-31insCT	ENSP00000512799.1:n.*272-32_*272-31insCT
ENST00000696683.1:c.3333-32_3333-31insCT
ENST00000696684.1:c.3333-32_3333-31insCT
ENST00000696685.1:c.3333-32_3333-31insCT
ENST00000696686.1:n.1253-32_1253-31insCT
ENST00000267430.10:c.4516-32_4516-31insCT MANE Select	ENSP00000267430.5:n.4516-32_4516-31insCT
ENST00000267430.9:c.4516-32_4516-31insCT	ENSP00000267430.5:n.4516-32_4516-31insCT
ENST00000542564.6:c.4438-32_4438-31insCT	ENSP00000442493.2:n.4438-32_4438-31insCT
ENST00000554809.5:c.1313-32_1313-31insCT
ENST00000555013.1:n.349-32_349-31insCT
ENST00000556250.5:c.3064-32_3064-31insCT	ENSP00000452033.1:n.3064-32_3064-31insCT
NM_001308133.1:c.4438-32_4438-31insCT	NP_001295062.1:n.4438-32_4438-31insCT
NM_020937.2:c.4516-32_4516-31insCT , LRG_502t1:c.4516-32_4516-31insCT	NP_065988.1:n.4516-32_4516-31insCT
NM_020937.3:c.4516-32_4516-31insCT	NP_065988.1:n.4516-32_4516-31insCT
XM_011537034.1:c.4531-32_4531-31insCT	XP_011535336.1:n.4531-32_4531-31insCT
XM_011537035.1:c.4453-32_4453-31insCT	XP_011535337.1:n.4453-32_4453-31insCT
XM_011537036.1:c.4531-32_4531-31insCT	XP_011535338.1:n.4531-32_4531-31insCT
XM_011537037.1:c.2545-32_2545-31insCT	XP_011535339.1:n.2545-32_2545-31insCT
XM_011537034.2:c.4531-32_4531-31insCT	XP_011535336.1:n.4531-32_4531-31insCT
XM_011537035.3:c.4453-32_4453-31insCT	XP_011535337.1:n.4453-32_4453-31insCT
XM_011537037.3:c.2545-32_2545-31insCT	XP_011535339.1:n.2545-32_2545-31insCT
XM_017021523.1:c.4531-32_4531-31insCT	XP_016877012.1:n.4531-32_4531-31insCT
XM_017021524.2:c.3568-32_3568-31insCT	XP_016877013.1:n.3568-32_3568-31insCT
XM_017021525.2:c.3346-32_3346-31insCT	XP_016877014.1:n.3346-32_3346-31insCT
XM_017021526.2:c.3346-32_3346-31insCT	XP_016877015.1:n.3346-32_3346-31insCT
XM_017021527.1:c.3331-32_3331-31insCT	XP_016877016.1:n.3331-32_3331-31insCT
XR_001750470.1:n.4623-32_4623-31insCT
XR_001750471.2:n.4608-32_4608-31insCT
XR_001750472.1:n.4660-32_4660-31insCT
NM_020937.4:c.4516-32_4516-31insCT MANE Select	NP_065988.1:n.4516-32_4516-31insCT
NM_001308133.2:c.4438-32_4438-31insCT	NP_001295062.1:n.4438-32_4438-31insCT