Canonical Allele Identifier: CA645294119
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 426620
ClinVar RCV Id: RCV000489396
dbSNP Id: rs1085307714

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13081681del , CM000681.2:g.13081681del GRCh38
NC_000019.9:g.13192495del , CM000681.1:g.13192495del GRCh37
NC_000019.8:g.13053495del NCBI36
NG_032925.2:g.90912del

Transcript Alleles

HGVS Amino-acid change
ENST00000358552.8:c.954del
ENST00000622520.2:c.1075+2946del ENSP00000481181.2:n.1075+2946del
ENST00000693124.1:c.773+6010del
ENST00000592199.6:c.1080del
ENST00000676441.1:c.1104del
ENST00000358552.7:c.966del
ENST00000360105.8:c.966del
ENST00000397661.6:c.1080del
ENST00000585382.5:c.*449del
ENST00000585575.5:c.1056del
ENST00000586797.5:c.*911del
ENST00000587260.1:c.1077del
ENST00000587760.5:c.1056del
ENST00000588228.5:c.939del
ENST00000592199.5:c.1080del
NM_001271043.2:c.1104del
NM_001271044.2:c.1056del
NM_002501.3:c.1080del
XM_005259917.3:c.1134del
XM_005259918.3:c.1080del
XM_005259919.3:c.1257del
XM_005259920.3:c.1056del
XM_005259921.3:c.1255+2946del XP_005259978.1:n.1255+2946del
XM_005259922.3:c.1132+6010del XP_005259979.1:n.1132+6010del
XM_006722760.2:c.1134del
XM_011528040.1:c.1128del
NM_001365902.1:c.1080del
NM_001365982.1:c.957del
NM_001365983.1:c.939del
NM_001365984.1:c.1077del
NM_001365985.1:c.1077del
XM_005259917.4:c.1134del
NM_001271044.3:c.1056del
NM_001365902.2:c.1080del
NM_001365982.2:c.957del
NM_001365983.2:c.939del
NM_001365984.2:c.1077del
NM_001365985.2:c.1077del
NM_002501.4:c.1080del
NM_001365902.3:c.1080del
NM_001378404.1:c.1056del
NM_001378405.1:c.1128del