Canonical Allele Identifier: CA404304333

Gene: NFIX

Linked Data

• MyVariant Identifiers: chr19:g.13192593A>G (hg19) ; chr19:g.13081779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081779A>G , CM000681.2:g.13081779A>G	GRCh38
NC_000019.9:g.13192593A>G , CM000681.1:g.13192593A>G	GRCh37
NC_000019.8:g.13053593A>G	NCBI36
NG_032925.2:g.91010A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358552.8:c.1052A>G	ENSP00000351354.5:p.His351Arg
ENST00000622520.2:c.1075+3044A>G	ENSP00000481181.2:n.1075+3044A>G
ENST00000693124.1:c.773+6108A>G
ENST00000592199.6:c.1178A>G MANE Select	ENSP00000467512.1:p.His393Arg
ENST00000676441.1:c.1202A>G	ENSP00000502554.1:p.His401Arg
ENST00000358552.7:c.1064A>G	ENSP00000351354.4:p.His355Arg
ENST00000360105.8:c.1064A>G	ENSP00000353219.4:p.His355Arg
ENST00000397661.6:c.1178A>G	ENSP00000380781.2:p.His393Arg
ENST00000585382.5:c.*547A>G	ENSP00000466605.1:n.*547A>G
ENST00000585575.5:c.1154A>G	ENSP00000468794.1:p.His385Arg
ENST00000586797.5:c.*1009A>G	ENSP00000467536.1:n.*1009A>G
ENST00000587260.1:c.1175A>G	ENSP00000467785.1:p.His392Arg
ENST00000587760.5:c.1154A>G	ENSP00000466389.1:p.His385Arg
ENST00000588228.5:c.1037A>G	ENSP00000466735.1:p.His346Arg
ENST00000592199.5:c.1178A>G	ENSP00000467512.1:p.His393Arg
NM_001271043.2:c.1202A>G	NP_001257972.1:p.His401Arg
NM_001271044.2:c.1154A>G	NP_001257973.1:p.His385Arg
NM_002501.3:c.1178A>G	NP_002492.2:p.His393Arg
XM_005259917.3:c.1232A>G	XP_005259974.1:p.His411Arg
XM_005259918.3:c.1178A>G	XP_005259975.1:p.His393Arg
XM_005259919.3:c.1355A>G	XP_005259976.1:p.His452Arg
XM_005259920.3:c.1154A>G	XP_005259977.1:p.His385Arg
XM_005259921.3:c.1255+3044A>G	XP_005259978.1:n.1255+3044A>G
XM_005259922.3:c.1132+6108A>G	XP_005259979.1:n.1132+6108A>G
XM_006722760.2:c.1232A>G	XP_006722823.1:p.His411Arg
XM_011528040.1:c.1226A>G	XP_011526342.1:p.His409Arg
NM_001365902.1:c.1178A>G	NP_001352831.1:p.His393Arg
NM_001365982.1:c.1055A>G	NP_001352911.1:p.His352Arg
NM_001365983.1:c.1037A>G	NP_001352912.1:p.His346Arg
NM_001365984.1:c.1175A>G	NP_001352913.1:p.His392Arg
NM_001365985.1:c.1175A>G	NP_001352914.1:p.His392Arg
XM_005259917.4:c.1232A>G	XP_005259974.1:p.His411Arg
NM_001271044.3:c.1154A>G	NP_001257973.1:p.His385Arg
NM_001365902.2:c.1178A>G	NP_001352831.1:p.His393Arg
NM_001365982.2:c.1055A>G	NP_001352911.1:p.His352Arg
NM_001365983.2:c.1037A>G	NP_001352912.1:p.His346Arg
NM_001365984.2:c.1175A>G	NP_001352913.1:p.His392Arg
NM_001365985.2:c.1175A>G	NP_001352914.1:p.His392Arg
NM_002501.4:c.1178A>G	NP_002492.2:p.His393Arg
NM_001365902.3:c.1178A>G MANE Select	NP_001352831.1:p.His393Arg
NM_001378404.1:c.1154A>G	NP_001365333.1:p.His385Arg
NM_001378405.1:c.1226A>G	NP_001365334.1:p.His409Arg