Canonical Allele Identifier: CA404314059
Gene: NFIX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13025273A>C , CM000681.2:g.13025273A>C GRCh38
NC_000019.9:g.13136087A>C , CM000681.1:g.13136087A>C GRCh37
NC_000019.8:g.12997087A>C NCBI36
NG_032925.2:g.34504A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000358552.8:c.277A>C ENSP00000351354.5:p.Thr93Pro
ENST00000622520.2:c.277A>C ENSP00000481181.2:p.Thr93Pro
ENST00000693124.1:c.98A>C
ENST00000592199.6:c.280A>C MANE Select ENSP00000467512.1:p.Thr94Pro
ENST00000676441.1:c.304A>C ENSP00000502554.1:p.Thr102Pro
ENST00000358552.7:c.289A>C ENSP00000351354.4:p.Thr97Pro
ENST00000360105.8:c.289A>C ENSP00000353219.4:p.Thr97Pro
ENST00000397661.6:c.280A>C ENSP00000380781.2:p.Thr94Pro
ENST00000585382.5:c.139A>C ENSP00000466605.1:p.Thr47Pro
ENST00000585575.5:c.256A>C ENSP00000468794.1:p.Thr86Pro
ENST00000586797.5:c.*111A>C ENSP00000467536.1:n.*111A>C
ENST00000586873.1:c.139A>C ENSP00000468707.1:p.Thr47Pro
ENST00000587260.1:c.277A>C ENSP00000467785.1:p.Thr93Pro
ENST00000587760.5:c.256A>C ENSP00000466389.1:p.Thr86Pro
ENST00000588228.5:c.139A>C ENSP00000466735.1:p.Thr47Pro
ENST00000590027.1:c.139A>C ENSP00000465616.1:p.Thr47Pro
ENST00000591028.1:c.328A>C ENSP00000465094.1:p.Thr110Pro
ENST00000592199.5:c.280A>C ENSP00000467512.1:p.Thr94Pro
NM_001271043.2:c.304A>C NP_001257972.1:p.Thr102Pro
NM_001271044.2:c.256A>C NP_001257973.1:p.Thr86Pro
NM_002501.3:c.280A>C NP_002492.2:p.Thr94Pro
XM_005259917.3:c.457A>C XP_005259974.1:p.Thr153Pro
XM_005259918.3:c.280A>C XP_005259975.1:p.Thr94Pro
XM_005259919.3:c.457A>C XP_005259976.1:p.Thr153Pro
XM_005259920.3:c.256A>C XP_005259977.1:p.Thr86Pro
XM_005259921.3:c.457A>C XP_005259978.1:p.Thr153Pro
XM_005259922.3:c.457A>C XP_005259979.1:p.Thr153Pro
XM_006722760.2:c.457A>C XP_006722823.1:p.Thr153Pro
XM_011528040.1:c.328A>C XP_011526342.1:p.Thr110Pro
NM_001365902.1:c.280A>C NP_001352831.1:p.Thr94Pro
NM_001365982.1:c.280A>C NP_001352911.1:p.Thr94Pro
NM_001365983.1:c.139A>C NP_001352912.1:p.Thr47Pro
NM_001365984.1:c.277A>C NP_001352913.1:p.Thr93Pro
NM_001365985.1:c.277A>C NP_001352914.1:p.Thr93Pro
XM_005259917.4:c.457A>C XP_005259974.1:p.Thr153Pro
NM_001271044.3:c.256A>C NP_001257973.1:p.Thr86Pro
NM_001365902.2:c.280A>C NP_001352831.1:p.Thr94Pro
NM_001365982.2:c.280A>C NP_001352911.1:p.Thr94Pro
NM_001365983.2:c.139A>C NP_001352912.1:p.Thr47Pro
NM_001365984.2:c.277A>C NP_001352913.1:p.Thr93Pro
NM_001365985.2:c.277A>C NP_001352914.1:p.Thr93Pro
NM_002501.4:c.280A>C NP_002492.2:p.Thr94Pro
NM_001365902.3:c.280A>C MANE Select NP_001352831.1:p.Thr94Pro
NM_001378404.1:c.256A>C NP_001365333.1:p.Thr86Pro
NM_001378405.1:c.328A>C NP_001365334.1:p.Thr110Pro