Canonical Allele Identifier: CA2323688853
Gene: NFIX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13025172T= , CM000681.2:g.13025172T= GRCh38
NC_000019.9:g.13135986T= , CM000681.1:g.13135986T= GRCh37
NC_000019.8:g.12996986T= NCBI36
NG_032925.2:g.34403T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358552.8:c.176T= ENSP00000351354.5:p.Leu59=
ENST00000622520.2:c.176T= ENSP00000481181.2:p.Leu59=
ENST00000592199.6:c.179T= MANE Select ENSP00000467512.1:p.Leu60=
ENST00000676441.1:c.203T= ENSP00000502554.1:p.Leu68=
ENST00000358552.7:c.188T= ENSP00000351354.4:p.Leu63=
ENST00000360105.8:c.188T= ENSP00000353219.4:p.Leu63=
ENST00000397661.6:c.179T= ENSP00000380781.2:p.Leu60=
ENST00000585382.5:c.38T= ENSP00000466605.1:p.Leu13=
ENST00000585575.5:c.155T= ENSP00000468794.1:p.Leu52=
ENST00000586797.5:c.*10T= ENSP00000467536.1:n.*10T=
ENST00000586873.1:c.38T= ENSP00000468707.1:p.Leu13=
ENST00000587260.1:c.176T= ENSP00000467785.1:p.Leu59=
ENST00000587760.5:c.155T= ENSP00000466389.1:p.Leu52=
ENST00000588228.5:c.38T= ENSP00000466735.1:p.Leu13=
ENST00000590027.1:c.38T= ENSP00000465616.1:p.Leu13=
ENST00000591028.1:c.227T= ENSP00000465094.1:p.Leu76=
ENST00000592199.5:c.179T= ENSP00000467512.1:p.Leu60=
NM_001271043.2:c.203T= NP_001257972.1:p.Leu68=
NM_001271044.2:c.155T= NP_001257973.1:p.Leu52=
NM_002501.3:c.179T= NP_002492.2:p.Leu60=
XM_005259917.3:c.356T= XP_005259974.1:p.Leu119=
XM_005259918.3:c.179T= XP_005259975.1:p.Leu60=
XM_005259919.3:c.356T= XP_005259976.1:p.Leu119=
XM_005259920.3:c.155T= XP_005259977.1:p.Leu52=
XM_005259921.3:c.356T= XP_005259978.1:p.Leu119=
XM_005259922.3:c.356T= XP_005259979.1:p.Leu119=
XM_006722760.2:c.356T= XP_006722823.1:p.Leu119=
XM_011528040.1:c.227T= XP_011526342.1:p.Leu76=
NM_001365902.1:c.179T= NP_001352831.1:p.Leu60=
NM_001365982.1:c.179T= NP_001352911.1:p.Leu60=
NM_001365983.1:c.38T= NP_001352912.1:p.Leu13=
NM_001365984.1:c.176T= NP_001352913.1:p.Leu59=
NM_001365985.1:c.176T= NP_001352914.1:p.Leu59=
XM_005259917.4:c.356T= XP_005259974.1:p.Leu119=
NM_001271044.3:c.155T= NP_001257973.1:p.Leu52=
NM_001365902.2:c.179T= NP_001352831.1:p.Leu60=
NM_001365982.2:c.179T= NP_001352911.1:p.Leu60=
NM_001365983.2:c.38T= NP_001352912.1:p.Leu13=
NM_001365984.2:c.176T= NP_001352913.1:p.Leu59=
NM_001365985.2:c.176T= NP_001352914.1:p.Leu59=
NM_002501.4:c.179T= NP_002492.2:p.Leu60=
NM_001365902.3:c.179T= MANE Select NP_001352831.1:p.Leu60=
NM_001378404.1:c.155T= NP_001365333.1:p.Leu52=
NM_001378405.1:c.227T= NP_001365334.1:p.Leu76=