Canonical Allele Identifier: CA2323688857
Gene: NFIX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13025180G= , CM000681.2:g.13025180G= GRCh38
NC_000019.9:g.13135994G= , CM000681.1:g.13135994G= GRCh37
NC_000019.8:g.12996994G= NCBI36
NG_032925.2:g.34411G=

Transcript Alleles

HGVS Amino-acid change
ENST00000358552.8:c.184G= ENSP00000351354.5:p.Glu62=
ENST00000622520.2:c.184G= ENSP00000481181.2:p.Glu62=
ENST00000693124.1:c.5G=
ENST00000592199.6:c.187G= MANE Select ENSP00000467512.1:p.Glu63=
ENST00000676441.1:c.211G= ENSP00000502554.1:p.Glu71=
ENST00000358552.7:c.196G= ENSP00000351354.4:p.Glu66=
ENST00000360105.8:c.196G= ENSP00000353219.4:p.Glu66=
ENST00000397661.6:c.187G= ENSP00000380781.2:p.Glu63=
ENST00000585382.5:c.46G= ENSP00000466605.1:p.Glu16=
ENST00000585575.5:c.163G= ENSP00000468794.1:p.Glu55=
ENST00000586797.5:c.*18G= ENSP00000467536.1:n.*18G=
ENST00000586873.1:c.46G= ENSP00000468707.1:p.Glu16=
ENST00000587260.1:c.184G= ENSP00000467785.1:p.Glu62=
ENST00000587760.5:c.163G= ENSP00000466389.1:p.Glu55=
ENST00000588228.5:c.46G= ENSP00000466735.1:p.Glu16=
ENST00000590027.1:c.46G= ENSP00000465616.1:p.Glu16=
ENST00000591028.1:c.235G= ENSP00000465094.1:p.Glu79=
ENST00000592199.5:c.187G= ENSP00000467512.1:p.Glu63=
NM_001271043.2:c.211G= NP_001257972.1:p.Glu71=
NM_001271044.2:c.163G= NP_001257973.1:p.Glu55=
NM_002501.3:c.187G= NP_002492.2:p.Glu63=
XM_005259917.3:c.364G= XP_005259974.1:p.Glu122=
XM_005259918.3:c.187G= XP_005259975.1:p.Glu63=
XM_005259919.3:c.364G= XP_005259976.1:p.Glu122=
XM_005259920.3:c.163G= XP_005259977.1:p.Glu55=
XM_005259921.3:c.364G= XP_005259978.1:p.Glu122=
XM_005259922.3:c.364G= XP_005259979.1:p.Glu122=
XM_006722760.2:c.364G= XP_006722823.1:p.Glu122=
XM_011528040.1:c.235G= XP_011526342.1:p.Glu79=
NM_001365902.1:c.187G= NP_001352831.1:p.Glu63=
NM_001365982.1:c.187G= NP_001352911.1:p.Glu63=
NM_001365983.1:c.46G= NP_001352912.1:p.Glu16=
NM_001365984.1:c.184G= NP_001352913.1:p.Glu62=
NM_001365985.1:c.184G= NP_001352914.1:p.Glu62=
XM_005259917.4:c.364G= XP_005259974.1:p.Glu122=
NM_001271044.3:c.163G= NP_001257973.1:p.Glu55=
NM_001365902.2:c.187G= NP_001352831.1:p.Glu63=
NM_001365982.2:c.187G= NP_001352911.1:p.Glu63=
NM_001365983.2:c.46G= NP_001352912.1:p.Glu16=
NM_001365984.2:c.184G= NP_001352913.1:p.Glu62=
NM_001365985.2:c.184G= NP_001352914.1:p.Glu62=
NM_002501.4:c.187G= NP_002492.2:p.Glu63=
NM_001365902.3:c.187G= MANE Select NP_001352831.1:p.Glu63=
NM_001378404.1:c.163G= NP_001365333.1:p.Glu55=
NM_001378405.1:c.235G= NP_001365334.1:p.Glu79=