Canonical Allele Identifier: CA2839381887

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081667del , CM000681.2:g.13081667del	GRCh38
NC_000019.9:g.13192481del , CM000681.1:g.13192481del	GRCh37
NC_000019.8:g.13053481del	NCBI36
NG_032925.2:g.90898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358552.8:c.953-13del	ENSP00000351354.5:n.953-13del
ENST00000622520.2:c.1075+2932del	ENSP00000481181.2:n.1075+2932del
ENST00000693124.1:c.773+5996del
ENST00000592199.6:c.1079-13del MANE Select	ENSP00000467512.1:n.1079-13del
ENST00000676441.1:c.1103-13del	ENSP00000502554.1:n.1103-13del
ENST00000358552.7:c.965-13del	ENSP00000351354.4:n.965-13del
ENST00000360105.8:c.965-13del	ENSP00000353219.4:n.965-13del
ENST00000397661.6:c.1079-13del	ENSP00000380781.2:n.1079-13del
ENST00000585382.5:c.*448-13del	ENSP00000466605.1:n.*448-13del
ENST00000585575.5:c.1055-13del	ENSP00000468794.1:n.1055-13del
ENST00000586797.5:c.*910-13del	ENSP00000467536.1:n.*910-13del
ENST00000587260.1:c.1076-13del	ENSP00000467785.1:n.1076-13del
ENST00000587760.5:c.1055-13del	ENSP00000466389.1:n.1055-13del
ENST00000588228.5:c.938-13del	ENSP00000466735.1:n.938-13del
ENST00000592199.5:c.1079-13del	ENSP00000467512.1:n.1079-13del
NM_001271043.2:c.1103-13del	NP_001257972.1:n.1103-13del
NM_001271044.2:c.1055-13del	NP_001257973.1:n.1055-13del
NM_002501.3:c.1079-13del	NP_002492.2:n.1079-13del
XM_005259917.3:c.1133-13del	XP_005259974.1:n.1133-13del
XM_005259918.3:c.1079-13del	XP_005259975.1:n.1079-13del
XM_005259919.3:c.1256-13del	XP_005259976.1:n.1256-13del
XM_005259920.3:c.1055-13del	XP_005259977.1:n.1055-13del
XM_005259921.3:c.1255+2932del	XP_005259978.1:n.1255+2932del
XM_005259922.3:c.1132+5996del	XP_005259979.1:n.1132+5996del
XM_006722760.2:c.1133-13del	XP_006722823.1:n.1133-13del
XM_011528040.1:c.1127-13del	XP_011526342.1:n.1127-13del
NM_001365902.1:c.1079-13del	NP_001352831.1:n.1079-13del
NM_001365982.1:c.956-13del	NP_001352911.1:n.956-13del
NM_001365983.1:c.938-13del	NP_001352912.1:n.938-13del
NM_001365984.1:c.1076-13del	NP_001352913.1:n.1076-13del
NM_001365985.1:c.1076-13del	NP_001352914.1:n.1076-13del
XM_005259917.4:c.1133-13del	XP_005259974.1:n.1133-13del
NM_001271044.3:c.1055-13del	NP_001257973.1:n.1055-13del
NM_001365902.2:c.1079-13del	NP_001352831.1:n.1079-13del
NM_001365982.2:c.956-13del	NP_001352911.1:n.956-13del
NM_001365983.2:c.938-13del	NP_001352912.1:n.938-13del
NM_001365984.2:c.1076-13del	NP_001352913.1:n.1076-13del
NM_001365985.2:c.1076-13del	NP_001352914.1:n.1076-13del
NM_002501.4:c.1079-13del	NP_002492.2:n.1079-13del
NM_001365902.3:c.1079-13del MANE Select	NP_001352831.1:n.1079-13del
NM_001378404.1:c.1055-13del	NP_001365333.1:n.1055-13del
NM_001378405.1:c.1127-13del	NP_001365334.1:n.1127-13del