Canonical Allele Identifier: CA404314738
Gene: NFIX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13025376G>A , CM000681.2:g.13025376G>A GRCh38
NC_000019.9:g.13136190G>A , CM000681.1:g.13136190G>A GRCh37
NC_000019.8:g.12997190G>A NCBI36
NG_032925.2:g.34607G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001365902.3:c.383G>A MANE Select NP_001352831.1:p.Arg128Gln
ENST00000592199.6:c.383G>A MANE Select ENSP00000467512.1:p.Arg128Gln
NM_001271043.2:c.407G>A NP_001257972.1:p.Arg136Gln
NM_001271044.2:c.359G>A NP_001257973.1:p.Arg120Gln
NM_001271044.3:c.359G>A NP_001257973.1:p.Arg120Gln
NM_001365902.1:c.383G>A NP_001352831.1:p.Arg128Gln
NM_001365902.2:c.383G>A NP_001352831.1:p.Arg128Gln
NM_001365982.1:c.383G>A NP_001352911.1:p.Arg128Gln
NM_001365982.2:c.383G>A NP_001352911.1:p.Arg128Gln
NM_001365983.1:c.242G>A NP_001352912.1:p.Arg81Gln
NM_001365983.2:c.242G>A NP_001352912.1:p.Arg81Gln
NM_001365984.1:c.380G>A NP_001352913.1:p.Arg127Gln
NM_001365984.2:c.380G>A NP_001352913.1:p.Arg127Gln
NM_001365985.1:c.380G>A NP_001352914.1:p.Arg127Gln
NM_001365985.2:c.380G>A NP_001352914.1:p.Arg127Gln
NM_001378404.1:c.359G>A NP_001365333.1:p.Arg120Gln
NM_001378405.1:c.431G>A NP_001365334.1:p.Arg144Gln
NM_002501.3:c.383G>A NP_002492.2:p.Arg128Gln
NM_002501.4:c.383G>A NP_002492.2:p.Arg128Gln
ENST00000358552.7:c.392G>A ENSP00000351354.4:p.Arg131Gln
ENST00000358552.8:c.380G>A ENSP00000351354.5:p.Arg127Gln
ENST00000360105.8:c.392G>A ENSP00000353219.4:p.Arg131Gln
ENST00000397661.6:c.383G>A ENSP00000380781.2:p.Arg128Gln
ENST00000585382.5:c.234+8G>A ENSP00000466605.1:n.234+8G>A
ENST00000585575.5:c.359G>A ENSP00000468794.1:p.Arg120Gln
ENST00000586797.5:c.*214G>A ENSP00000467536.1:n.*214G>A
ENST00000586873.1:c.242G>A ENSP00000468707.1:p.Arg81Gln
ENST00000587260.1:c.380G>A ENSP00000467785.1:p.Arg127Gln
ENST00000587760.5:c.359G>A ENSP00000466389.1:p.Arg120Gln
ENST00000588228.5:c.242G>A ENSP00000466735.1:p.Arg81Gln
ENST00000590027.1:c.242G>A ENSP00000465616.1:p.Arg81Gln
ENST00000591028.1:c.431G>A ENSP00000465094.1:p.Arg144Gln
ENST00000592199.5:c.383G>A ENSP00000467512.1:p.Arg128Gln
ENST00000622520.2:c.380G>A ENSP00000481181.2:p.Arg127Gln
ENST00000676441.1:c.407G>A ENSP00000502554.1:p.Arg136Gln
ENST00000693124.1:c.201G>A
XM_005259917.3:c.560G>A XP_005259974.1:p.Arg187Gln
XM_005259917.4:c.560G>A XP_005259974.1:p.Arg187Gln
XM_005259918.3:c.383G>A XP_005259975.1:p.Arg128Gln
XM_005259919.3:c.560G>A XP_005259976.1:p.Arg187Gln
XM_005259920.3:c.359G>A XP_005259977.1:p.Arg120Gln
XM_005259921.3:c.560G>A XP_005259978.1:p.Arg187Gln
XM_005259922.3:c.560G>A XP_005259979.1:p.Arg187Gln
XM_006722760.2:c.560G>A XP_006722823.1:p.Arg187Gln
XM_011528040.1:c.431G>A XP_011526342.1:p.Arg144Gln