Canonical Allele Identifier: CA2624697903

Gene: FANCM

Linked Data

• gnomAD v4: 14-45159209-A-ACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159209_45159210insCTC , CM000676.2:g.45159209_45159210insCTC	GRCh38
NC_000014.8:g.45628412_45628413insCTC , CM000676.1:g.45628412_45628413insCTC	GRCh37
NC_000014.7:g.44698162_44698163insCTC	NCBI36
NG_007417.1:g.28277_28278insCTC , LRG_502:g.28277_28278insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1510_1511insCTC	ENSP00000450596.1:p.Ile503_Arg504insThr
ENST00000556250.6:c.1510_1511insCTC	ENSP00000452033.2:p.Ile503_Arg504insThr
ENST00000696641.1:c.1351_1352insCTC	ENSP00000512774.1:p.Ile450_Arg451insThr
ENST00000696642.1:c.*321_*322insCTC	ENSP00000512775.1:n.*321_*322insCTC
ENST00000696643.1:c.1510_1511insCTC	ENSP00000512776.1:p.Ile503_Arg504insThr
ENST00000696646.1:c.*321_*322insCTC	ENSP00000512777.1:n.*321_*322insCTC
ENST00000696647.1:c.1510_1511insCTC	ENSP00000512778.1:p.Ile503_Arg504insThr
ENST00000696648.1:c.1510_1511insCTC	ENSP00000512779.1:p.Ile503_Arg504insThr
ENST00000696649.1:c.1510_1511insCTC	ENSP00000512780.1:p.Ile503_Arg504insThr
ENST00000696650.1:n.1458_1459insCTC
ENST00000696658.1:n.2060_2061insCTC
ENST00000696662.1:c.1432_1433insCTC	ENSP00000512788.1:p.Ile477_Arg478insThr
ENST00000696663.1:c.327_328insCTC
ENST00000696664.1:c.327_328insCTC
ENST00000696675.1:c.1510_1511insCTC	ENSP00000512799.1:p.Ile503_Arg504insThr
ENST00000696680.1:c.1378_1379insCTC	ENSP00000512803.1:p.Ile459_Arg460insThr
ENST00000696681.1:c.*321_*322insCTC	ENSP00000512804.1:n.*321_*322insCTC
ENST00000696682.1:c.1510_1511insCTC	ENSP00000512805.1:p.Ile503_Arg504insThr
ENST00000696683.1:c.327_328insCTC
ENST00000696684.1:c.327_328insCTC
ENST00000696685.1:c.327_328insCTC
ENST00000267430.10:c.1510_1511insCTC MANE Select	ENSP00000267430.5:p.Ile503_Arg504insThr
ENST00000267430.9:c.1510_1511insCTC	ENSP00000267430.5:p.Ile503_Arg504insThr
ENST00000542564.6:c.1432_1433insCTC	ENSP00000442493.2:p.Ile477_Arg478insThr
ENST00000556036.5:c.1510_1511insCTC	ENSP00000450596.1:p.Ile503_Arg504insThr
ENST00000556250.5:c.265_266insCTC	ENSP00000452033.1:p.Ile88_Arg89insThr
NM_001308133.1:c.1432_1433insCTC	NP_001295062.1:p.Ile477_Arg478insThr
NM_001308134.1:c.1510_1511insCTC	NP_001295063.1:p.Ile503_Arg504insThr
NM_020937.2:c.1510_1511insCTC , LRG_502t1:c.1510_1511insCTC	NP_065988.1:p.Ile503_Arg504insThr
NM_020937.3:c.1510_1511insCTC	NP_065988.1:p.Ile503_Arg504insThr
XM_011537034.1:c.1510_1511insCTC	XP_011535336.1:p.Ile503_Arg504insThr
XM_011537035.1:c.1432_1433insCTC	XP_011535337.1:p.Ile477_Arg478insThr
XM_011537036.1:c.1510_1511insCTC	XP_011535338.1:p.Ile503_Arg504insThr
XM_011537034.2:c.1510_1511insCTC	XP_011535336.1:p.Ile503_Arg504insThr
XM_011537035.3:c.1432_1433insCTC	XP_011535337.1:p.Ile477_Arg478insThr
XM_017021523.1:c.1510_1511insCTC	XP_016877012.1:p.Ile503_Arg504insThr
XM_017021524.2:c.547_548insCTC	XP_016877013.1:p.Ile182_Arg183insThr
XM_017021525.2:c.325_326insCTC	XP_016877014.1:p.Ile108_Arg109insThr
XM_017021526.2:c.325_326insCTC	XP_016877015.1:p.Ile108_Arg109insThr
XM_017021527.1:c.325_326insCTC	XP_016877016.1:p.Ile108_Arg109insThr
XR_001750470.1:n.1602_1603insCTC
XR_001750471.2:n.1602_1603insCTC
XR_001750472.1:n.1602_1603insCTC
NM_020937.4:c.1510_1511insCTC MANE Select	NP_065988.1:p.Ile503_Arg504insThr
NM_001308133.2:c.1432_1433insCTC	NP_001295062.1:p.Ile477_Arg478insThr
NM_001308134.2:c.1510_1511insCTC	NP_001295063.1:p.Ile503_Arg504insThr