Canonical Allele Identifier: CA2813656097

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13025343_13025360del , CM000681.2:g.13025343_13025360del	GRCh38
NC_000019.9:g.13136157_13136174del , CM000681.1:g.13136157_13136174del	GRCh37
NC_000019.8:g.12997157_12997174del	NCBI36
NG_032925.2:g.34574_34591del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358552.8:c.347_364del	ENSP00000351354.5:p.Ile116_Ala122delinsThr
ENST00000622520.2:c.347_364del	ENSP00000481181.2:p.Ile116_Ala122delinsThr
ENST00000693124.1:c.168_185del
ENST00000592199.6:c.350_367del MANE Select	ENSP00000467512.1:p.Ile117_Ala123delinsThr
ENST00000676441.1:c.374_391del	ENSP00000502554.1:p.Ile125_Ala131delinsThr
ENST00000358552.7:c.359_376del	ENSP00000351354.4:p.Ile120_Ala126delinsThr
ENST00000360105.8:c.359_376del	ENSP00000353219.4:p.Ile120_Ala126delinsThr
ENST00000397661.6:c.350_367del	ENSP00000380781.2:p.Ile117_Ala123delinsThr
ENST00000585382.5:c.209_226del	ENSP00000466605.1:p.Ile70_Ala76delinsThr
ENST00000585575.5:c.326_343del	ENSP00000468794.1:p.Ile109_Ala115delinsThr
ENST00000586797.5:c.*181_*198del	ENSP00000467536.1:n.*181_*198del
ENST00000586873.1:c.209_226del	ENSP00000468707.1:p.Ile70_Ala76delinsThr
ENST00000587260.1:c.347_364del	ENSP00000467785.1:p.Ile116_Ala122delinsThr
ENST00000587760.5:c.326_343del	ENSP00000466389.1:p.Ile109_Ala115delinsThr
ENST00000588228.5:c.209_226del	ENSP00000466735.1:p.Ile70_Ala76delinsThr
ENST00000590027.1:c.209_226del	ENSP00000465616.1:p.Ile70_Ala76delinsThr
ENST00000591028.1:c.398_415del	ENSP00000465094.1:p.Ile133_Ala139delinsThr
ENST00000592199.5:c.350_367del	ENSP00000467512.1:p.Ile117_Ala123delinsThr
NM_001271043.2:c.374_391del	NP_001257972.1:p.Ile125_Ala131delinsThr
NM_001271044.2:c.326_343del	NP_001257973.1:p.Ile109_Ala115delinsThr
NM_002501.3:c.350_367del	NP_002492.2:p.Ile117_Ala123delinsThr
XM_005259917.3:c.527_544del	XP_005259974.1:p.Ile176_Ala182delinsThr
XM_005259918.3:c.350_367del	XP_005259975.1:p.Ile117_Ala123delinsThr
XM_005259919.3:c.527_544del	XP_005259976.1:p.Ile176_Ala182delinsThr
XM_005259920.3:c.326_343del	XP_005259977.1:p.Ile109_Ala115delinsThr
XM_005259921.3:c.527_544del	XP_005259978.1:p.Ile176_Ala182delinsThr
XM_005259922.3:c.527_544del	XP_005259979.1:p.Ile176_Ala182delinsThr
XM_006722760.2:c.527_544del	XP_006722823.1:p.Ile176_Ala182delinsThr
XM_011528040.1:c.398_415del	XP_011526342.1:p.Ile133_Ala139delinsThr
NM_001365902.1:c.350_367del	NP_001352831.1:p.Ile117_Ala123delinsThr
NM_001365982.1:c.350_367del	NP_001352911.1:p.Ile117_Ala123delinsThr
NM_001365983.1:c.209_226del	NP_001352912.1:p.Ile70_Ala76delinsThr
NM_001365984.1:c.347_364del	NP_001352913.1:p.Ile116_Ala122delinsThr
NM_001365985.1:c.347_364del	NP_001352914.1:p.Ile116_Ala122delinsThr
XM_005259917.4:c.527_544del	XP_005259974.1:p.Ile176_Ala182delinsThr
NM_001271044.3:c.326_343del	NP_001257973.1:p.Ile109_Ala115delinsThr
NM_001365902.2:c.350_367del	NP_001352831.1:p.Ile117_Ala123delinsThr
NM_001365982.2:c.350_367del	NP_001352911.1:p.Ile117_Ala123delinsThr
NM_001365983.2:c.209_226del	NP_001352912.1:p.Ile70_Ala76delinsThr
NM_001365984.2:c.347_364del	NP_001352913.1:p.Ile116_Ala122delinsThr
NM_001365985.2:c.347_364del	NP_001352914.1:p.Ile116_Ala122delinsThr
NM_002501.4:c.350_367del	NP_002492.2:p.Ile117_Ala123delinsThr
NM_001365902.3:c.350_367del MANE Select	NP_001352831.1:p.Ile117_Ala123delinsThr
NM_001378404.1:c.326_343del	NP_001365333.1:p.Ile109_Ala115delinsThr
NM_001378405.1:c.398_415del	NP_001365334.1:p.Ile133_Ala139delinsThr