Canonical Allele Identifier: CA2323714197

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081721A= , CM000681.2:g.13081721A=	GRCh38
NC_000019.9:g.13192535A= , CM000681.1:g.13192535A=	GRCh37
NC_000019.8:g.13053535A=	NCBI36
NG_032925.2:g.90952A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358552.8:c.994A=	ENSP00000351354.5:p.Thr332=
ENST00000622520.2:c.1075+2986A=	ENSP00000481181.2:n.1075+2986A=
ENST00000693124.1:c.773+6050A=
ENST00000592199.6:c.1120A= MANE Select	ENSP00000467512.1:p.Thr374=
ENST00000676441.1:c.1144A=	ENSP00000502554.1:p.Thr382=
ENST00000358552.7:c.1006A=	ENSP00000351354.4:p.Thr336=
ENST00000360105.8:c.1006A=	ENSP00000353219.4:p.Thr336=
ENST00000397661.6:c.1120A=	ENSP00000380781.2:p.Thr374=
ENST00000585382.5:c.*489A=	ENSP00000466605.1:n.*489A=
ENST00000585575.5:c.1096A=	ENSP00000468794.1:p.Thr366=
ENST00000586797.5:c.*951A=	ENSP00000467536.1:n.*951A=
ENST00000587260.1:c.1117A=	ENSP00000467785.1:p.Thr373=
ENST00000587760.5:c.1096A=	ENSP00000466389.1:p.Thr366=
ENST00000588228.5:c.979A=	ENSP00000466735.1:p.Thr327=
ENST00000592199.5:c.1120A=	ENSP00000467512.1:p.Thr374=
NM_001271043.2:c.1144A=	NP_001257972.1:p.Thr382=
NM_001271044.2:c.1096A=	NP_001257973.1:p.Thr366=
NM_002501.3:c.1120A=	NP_002492.2:p.Thr374=
XM_005259917.3:c.1174A=	XP_005259974.1:p.Thr392=
XM_005259918.3:c.1120A=	XP_005259975.1:p.Thr374=
XM_005259919.3:c.1297A=	XP_005259976.1:p.Thr433=
XM_005259920.3:c.1096A=	XP_005259977.1:p.Thr366=
XM_005259921.3:c.1255+2986A=	XP_005259978.1:n.1255+2986A=
XM_005259922.3:c.1132+6050A=	XP_005259979.1:n.1132+6050A=
XM_006722760.2:c.1174A=	XP_006722823.1:p.Thr392=
XM_011528040.1:c.1168A=	XP_011526342.1:p.Thr390=
NM_001365902.1:c.1120A=	NP_001352831.1:p.Thr374=
NM_001365982.1:c.997A=	NP_001352911.1:p.Thr333=
NM_001365983.1:c.979A=	NP_001352912.1:p.Thr327=
NM_001365984.1:c.1117A=	NP_001352913.1:p.Thr373=
NM_001365985.1:c.1117A=	NP_001352914.1:p.Thr373=
XM_005259917.4:c.1174A=	XP_005259974.1:p.Thr392=
NM_001271044.3:c.1096A=	NP_001257973.1:p.Thr366=
NM_001365902.2:c.1120A=	NP_001352831.1:p.Thr374=
NM_001365982.2:c.997A=	NP_001352911.1:p.Thr333=
NM_001365983.2:c.979A=	NP_001352912.1:p.Thr327=
NM_001365984.2:c.1117A=	NP_001352913.1:p.Thr373=
NM_001365985.2:c.1117A=	NP_001352914.1:p.Thr373=
NM_002501.4:c.1120A=	NP_002492.2:p.Thr374=
NM_001365902.3:c.1120A= MANE Select	NP_001352831.1:p.Thr374=
NM_001378404.1:c.1096A=	NP_001365333.1:p.Thr366=
NM_001378405.1:c.1168A=	NP_001365334.1:p.Thr390=