Canonical Allele Identifier: CA915952490
Gene: NFIX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13075649_13075659del , CM000681.2:g.13075649_13075659del GRCh38
NC_000019.9:g.13186463_13186473del , CM000681.1:g.13186463_13186473del GRCh37
NC_000019.8:g.13047463_13047473del NCBI36
NG_032925.2:g.84880_84890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358552.8:c.930_940del ENSP00000351354.5:p.Trp311CysfsTer?
ENST00000622520.2:c.930_940del ENSP00000481181.2:p.Trp311CysfsTer?
ENST00000693124.1:c.751_761del
ENST00000592199.6:c.933_943del MANE Select ENSP00000467512.1:p.Trp312CysfsTer?
ENST00000676441.1:c.957_967del ENSP00000502554.1:p.Trp320CysfsTer?
ENST00000358552.7:c.942_952del ENSP00000351354.4:p.Trp315CysfsTer?
ENST00000360105.8:c.942_952del ENSP00000353219.4:p.Trp315CysfsTer?
ENST00000397661.6:c.933_943del ENSP00000380781.2:p.Trp312CysfsTer?
ENST00000585382.5:c.*302_*312del ENSP00000466605.1:n.*302_*312del
ENST00000585575.5:c.909_919del ENSP00000468794.1:p.Trp304CysfsTer?
ENST00000586797.5:c.*764_*774del ENSP00000467536.1:n.*764_*774del
ENST00000587260.1:c.930_940del ENSP00000467785.1:p.Trp311CysfsTer?
ENST00000587760.5:c.909_919del ENSP00000466389.1:p.Trp304CysfsTer?
ENST00000588228.5:c.792_802del ENSP00000466735.1:p.Trp265CysfsTer?
ENST00000592199.5:c.933_943del ENSP00000467512.1:p.Trp312CysfsTer?
NM_001271043.2:c.957_967del NP_001257972.1:p.Trp320CysfsTer?
NM_001271044.2:c.909_919del NP_001257973.1:p.Trp304CysfsTer?
NM_002501.3:c.933_943del NP_002492.2:p.Trp312CysfsTer?
XM_005259917.3:c.1110_1120del XP_005259974.1:p.Trp371CysfsTer?
XM_005259918.3:c.933_943del XP_005259975.1:p.Trp312CysfsTer?
XM_005259919.3:c.1110_1120del XP_005259976.1:p.Trp371CysfsTer?
XM_005259920.3:c.909_919del XP_005259977.1:p.Trp304CysfsTer?
XM_005259921.3:c.1110_1120del XP_005259978.1:p.Trp371CysfsTer?
XM_005259922.3:c.1110_1120del XP_005259979.1:p.Trp371CysfsTer?
XM_006722760.2:c.1110_1120del XP_006722823.1:p.Trp371CysfsTer?
XM_011528040.1:c.981_991del XP_011526342.1:p.Trp328CysfsTer?
NM_001365902.1:c.933_943del NP_001352831.1:p.Trp312CysfsTer?
NM_001365982.1:c.933_943del NP_001352911.1:p.Trp312CysfsTer?
NM_001365983.1:c.792_802del NP_001352912.1:p.Trp265CysfsTer?
NM_001365984.1:c.930_940del NP_001352913.1:p.Trp311CysfsTer?
NM_001365985.1:c.930_940del NP_001352914.1:p.Trp311CysfsTer?
XM_005259917.4:c.1110_1120del XP_005259974.1:p.Trp371CysfsTer?
NM_001271044.3:c.909_919del NP_001257973.1:p.Trp304CysfsTer?
NM_001365902.2:c.933_943del NP_001352831.1:p.Trp312CysfsTer?
NM_001365982.2:c.933_943del NP_001352911.1:p.Trp312CysfsTer?
NM_001365983.2:c.792_802del NP_001352912.1:p.Trp265CysfsTer?
NM_001365984.2:c.930_940del NP_001352913.1:p.Trp311CysfsTer?
NM_001365985.2:c.930_940del NP_001352914.1:p.Trp311CysfsTer?
NM_002501.4:c.933_943del NP_002492.2:p.Trp312CysfsTer?
NM_001365902.3:c.933_943del MANE Select NP_001352831.1:p.Trp312CysfsTer?
NM_001378404.1:c.909_919del NP_001365333.1:p.Trp304CysfsTer?
NM_001378405.1:c.981_991del NP_001365334.1:p.Trp328CysfsTer?