Canonical Allele Identifier: CA645604836

Gene: NFIX

Linked Data

• COSMIC: COSM4515440 ; COSM4515441 ; COSM4515442

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081687_13081688delinsTT , CM000681.2:g.13081687_13081688delinsTT	GRCh38
NC_000019.9:g.13192501_13192502delinsTT , CM000681.1:g.13192501_13192502delinsTT	GRCh37
NC_000019.8:g.13053501_13053502delinsTT	NCBI36
NG_032925.2:g.90918_90919delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000358552.8:c.960_961delinsTT	ENSP00000351354.5:p.Arg321Trp
ENST00000622520.2:c.1075+2952_1075+2953delinsTT	ENSP00000481181.2:n.1075+2952_1075+2953de...
ENST00000693124.1:c.773+6016_773+6017delinsTT
ENST00000592199.6:c.1086_1087delinsTT MANE Select	ENSP00000467512.1:p.Arg363Trp
ENST00000676441.1:c.1110_1111delinsTT	ENSP00000502554.1:p.Arg371Trp
ENST00000358552.7:c.972_973delinsTT	ENSP00000351354.4:p.Arg325Trp
ENST00000360105.8:c.972_973delinsTT	ENSP00000353219.4:p.Arg325Trp
ENST00000397661.6:c.1086_1087delinsTT	ENSP00000380781.2:p.Arg363Trp
ENST00000585382.5:c.*455_*456delinsTT	ENSP00000466605.1:n.*455_*456delinsTT
ENST00000585575.5:c.1062_1063delinsTT	ENSP00000468794.1:p.Arg355Trp
ENST00000586797.5:c.*917_*918delinsTT	ENSP00000467536.1:n.*917_*918delinsTT
ENST00000587260.1:c.1083_1084delinsTT	ENSP00000467785.1:p.Arg362Trp
ENST00000587760.5:c.1062_1063delinsTT	ENSP00000466389.1:p.Arg355Trp
ENST00000588228.5:c.945_946delinsTT	ENSP00000466735.1:p.Arg316Trp
ENST00000592199.5:c.1086_1087delinsTT	ENSP00000467512.1:p.Arg363Trp
NM_001271043.2:c.1110_1111delinsTT	NP_001257972.1:p.Arg371Trp
NM_001271044.2:c.1062_1063delinsTT	NP_001257973.1:p.Arg355Trp
NM_002501.3:c.1086_1087delinsTT	NP_002492.2:p.Arg363Trp
XM_005259917.3:c.1140_1141delinsTT	XP_005259974.1:p.Arg381Trp
XM_005259918.3:c.1086_1087delinsTT	XP_005259975.1:p.Arg363Trp
XM_005259919.3:c.1263_1264delinsTT	XP_005259976.1:p.Arg422Trp
XM_005259920.3:c.1062_1063delinsTT	XP_005259977.1:p.Arg355Trp
XM_005259921.3:c.1255+2952_1255+2953delinsTT	XP_005259978.1:n.1255+2952_1255+2953delin...
XM_005259922.3:c.1132+6016_1132+6017delinsTT	XP_005259979.1:n.1132+6016_1132+6017delin...
XM_006722760.2:c.1140_1141delinsTT	XP_006722823.1:p.Arg381Trp
XM_011528040.1:c.1134_1135delinsTT	XP_011526342.1:p.Arg379Trp
NM_001365902.1:c.1086_1087delinsTT	NP_001352831.1:p.Arg363Trp
NM_001365982.1:c.963_964delinsTT	NP_001352911.1:p.Arg322Trp
NM_001365983.1:c.945_946delinsTT	NP_001352912.1:p.Arg316Trp
NM_001365984.1:c.1083_1084delinsTT	NP_001352913.1:p.Arg362Trp
NM_001365985.1:c.1083_1084delinsTT	NP_001352914.1:p.Arg362Trp
XM_005259917.4:c.1140_1141delinsTT	XP_005259974.1:p.Arg381Trp
NM_001271044.3:c.1062_1063delinsTT	NP_001257973.1:p.Arg355Trp
NM_001365902.2:c.1086_1087delinsTT	NP_001352831.1:p.Arg363Trp
NM_001365982.2:c.963_964delinsTT	NP_001352911.1:p.Arg322Trp
NM_001365983.2:c.945_946delinsTT	NP_001352912.1:p.Arg316Trp
NM_001365984.2:c.1083_1084delinsTT	NP_001352913.1:p.Arg362Trp
NM_001365985.2:c.1083_1084delinsTT	NP_001352914.1:p.Arg362Trp
NM_002501.4:c.1086_1087delinsTT	NP_002492.2:p.Arg363Trp
NM_001365902.3:c.1086_1087delinsTT MANE Select	NP_001352831.1:p.Arg363Trp
NM_001378404.1:c.1062_1063delinsTT	NP_001365333.1:p.Arg355Trp
NM_001378405.1:c.1134_1135delinsTT	NP_001365334.1:p.Arg379Trp