Canonical Allele Identifier: CA2580096566

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081770_13081775dup , CM000681.2:g.13081770_13081775dup	GRCh38
NC_000019.9:g.13192584_13192589dup , CM000681.1:g.13192584_13192589dup	GRCh37
NC_000019.8:g.13053584_13053589dup	NCBI36
NG_032925.2:g.91001_91006dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001365902.3:c.1169_1174dup MANE Select	NP_001352831.1:p.Tyr391_His392insArgTyr
ENST00000592199.6:c.1169_1174dup MANE Select	ENSP00000467512.1:p.Tyr391_His392insArgTyr
NM_001271043.2:c.1193_1198dup	NP_001257972.1:p.Tyr399_His400insArgTyr
NM_001271044.2:c.1145_1150dup	NP_001257973.1:p.Tyr383_His384insArgTyr
NM_001271044.3:c.1145_1150dup	NP_001257973.1:p.Tyr383_His384insArgTyr
NM_001365902.1:c.1169_1174dup	NP_001352831.1:p.Tyr391_His392insArgTyr
NM_001365902.2:c.1169_1174dup	NP_001352831.1:p.Tyr391_His392insArgTyr
NM_001365982.1:c.1046_1051dup	NP_001352911.1:p.Tyr350_His351insArgTyr
NM_001365982.2:c.1046_1051dup	NP_001352911.1:p.Tyr350_His351insArgTyr
NM_001365983.1:c.1028_1033dup	NP_001352912.1:p.Tyr344_His345insArgTyr
NM_001365983.2:c.1028_1033dup	NP_001352912.1:p.Tyr344_His345insArgTyr
NM_001365984.1:c.1166_1171dup	NP_001352913.1:p.Tyr390_His391insArgTyr
NM_001365984.2:c.1166_1171dup	NP_001352913.1:p.Tyr390_His391insArgTyr
NM_001365985.1:c.1166_1171dup	NP_001352914.1:p.Tyr390_His391insArgTyr
NM_001365985.2:c.1166_1171dup	NP_001352914.1:p.Tyr390_His391insArgTyr
NM_001378404.1:c.1145_1150dup	NP_001365333.1:p.Tyr383_His384insArgTyr
NM_001378405.1:c.1217_1222dup	NP_001365334.1:p.Tyr407_His408insArgTyr
NM_002501.3:c.1169_1174dup	NP_002492.2:p.Tyr391_His392insArgTyr
NM_002501.4:c.1169_1174dup	NP_002492.2:p.Tyr391_His392insArgTyr
ENST00000358552.7:c.1055_1060dup	ENSP00000351354.4:p.Tyr353_His354insArgTyr
ENST00000358552.8:c.1043_1048dup	ENSP00000351354.5:p.Tyr349_His350insArgTyr
ENST00000360105.8:c.1055_1060dup	ENSP00000353219.4:p.Tyr353_His354insArgTyr
ENST00000397661.6:c.1169_1174dup	ENSP00000380781.2:p.Tyr391_His392insArgTyr
ENST00000585382.5:c.*538_*543dup	ENSP00000466605.1:n.*538_*543dup
ENST00000585575.5:c.1145_1150dup	ENSP00000468794.1:p.Tyr383_His384insArgTyr
ENST00000586797.5:c.*1000_*1005dup	ENSP00000467536.1:n.*1000_*1005dup
ENST00000587260.1:c.1166_1171dup	ENSP00000467785.1:p.Tyr390_His391insArgTyr
ENST00000587760.5:c.1145_1150dup	ENSP00000466389.1:p.Tyr383_His384insArgTyr
ENST00000588228.5:c.1028_1033dup	ENSP00000466735.1:p.Tyr344_His345insArgTyr
ENST00000592199.5:c.1169_1174dup	ENSP00000467512.1:p.Tyr391_His392insArgTyr
ENST00000622520.2:c.1075+3035_1075+3040dup	ENSP00000481181.2:n.1075+3035_1075+3040dup
ENST00000676441.1:c.1193_1198dup	ENSP00000502554.1:p.Tyr399_His400insArgTyr
ENST00000693124.1:c.773+6099_773+6104dup
XM_005259917.3:c.1223_1228dup	XP_005259974.1:p.Tyr409_His410insArgTyr
XM_005259917.4:c.1223_1228dup	XP_005259974.1:p.Tyr409_His410insArgTyr
XM_005259918.3:c.1169_1174dup	XP_005259975.1:p.Tyr391_His392insArgTyr
XM_005259919.3:c.1346_1351dup	XP_005259976.1:p.Tyr450_His451insArgTyr
XM_005259920.3:c.1145_1150dup	XP_005259977.1:p.Tyr383_His384insArgTyr
XM_005259921.3:c.1255+3035_1255+3040dup	XP_005259978.1:n.1255+3035_1255+3040dup
XM_005259922.3:c.1132+6099_1132+6104dup	XP_005259979.1:n.1132+6099_1132+6104dup
XM_006722760.2:c.1223_1228dup	XP_006722823.1:p.Tyr409_His410insArgTyr
XM_011528040.1:c.1217_1222dup	XP_011526342.1:p.Tyr407_His408insArgTyr