Canonical Allele Identifier: CA404315682

Gene: NFIX

Linked Data

• MyVariant Identifiers: chr19:g.13136301C>G (hg19) ; chr19:g.13025487C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13025487C>G , CM000681.2:g.13025487C>G	GRCh38
NC_000019.9:g.13136301C>G , CM000681.1:g.13136301C>G	GRCh37
NC_000019.8:g.12997301C>G	NCBI36
NG_032925.2:g.34718C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358552.8:c.491C>G	ENSP00000351354.5:p.Pro164Arg
ENST00000622520.2:c.491C>G	ENSP00000481181.2:p.Pro164Arg
ENST00000693124.1:c.312C>G
ENST00000592199.6:c.494C>G MANE Select	ENSP00000467512.1:p.Pro165Arg
ENST00000676441.1:c.518C>G	ENSP00000502554.1:p.Pro173Arg
ENST00000358552.7:c.503C>G	ENSP00000351354.4:p.Pro168Arg
ENST00000360105.8:c.503C>G	ENSP00000353219.4:p.Pro168Arg
ENST00000397661.6:c.494C>G	ENSP00000380781.2:p.Pro165Arg
ENST00000585382.5:c.234+119C>G	ENSP00000466605.1:n.234+119C>G
ENST00000585575.5:c.470C>G	ENSP00000468794.1:p.Pro157Arg
ENST00000586797.5:c.*325C>G	ENSP00000467536.1:n.*325C>G
ENST00000586873.1:c.353C>G	ENSP00000468707.1:p.Pro118Arg
ENST00000587260.1:c.491C>G	ENSP00000467785.1:p.Pro164Arg
ENST00000587760.5:c.470C>G	ENSP00000466389.1:p.Pro157Arg
ENST00000588228.5:c.353C>G	ENSP00000466735.1:p.Pro118Arg
ENST00000590027.1:c.353C>G	ENSP00000465616.1:p.Pro118Arg
ENST00000591028.1:c.542C>G	ENSP00000465094.1:p.Pro181Arg
ENST00000592199.5:c.494C>G	ENSP00000467512.1:p.Pro165Arg
NM_001271043.2:c.518C>G	NP_001257972.1:p.Pro173Arg
NM_001271044.2:c.470C>G	NP_001257973.1:p.Pro157Arg
NM_002501.3:c.494C>G	NP_002492.2:p.Pro165Arg
XM_005259917.3:c.671C>G	XP_005259974.1:p.Pro224Arg
XM_005259918.3:c.494C>G	XP_005259975.1:p.Pro165Arg
XM_005259919.3:c.671C>G	XP_005259976.1:p.Pro224Arg
XM_005259920.3:c.470C>G	XP_005259977.1:p.Pro157Arg
XM_005259921.3:c.671C>G	XP_005259978.1:p.Pro224Arg
XM_005259922.3:c.671C>G	XP_005259979.1:p.Pro224Arg
XM_006722760.2:c.671C>G	XP_006722823.1:p.Pro224Arg
XM_011528040.1:c.542C>G	XP_011526342.1:p.Pro181Arg
NM_001365902.1:c.494C>G	NP_001352831.1:p.Pro165Arg
NM_001365982.1:c.494C>G	NP_001352911.1:p.Pro165Arg
NM_001365983.1:c.353C>G	NP_001352912.1:p.Pro118Arg
NM_001365984.1:c.491C>G	NP_001352913.1:p.Pro164Arg
NM_001365985.1:c.491C>G	NP_001352914.1:p.Pro164Arg
XM_005259917.4:c.671C>G	XP_005259974.1:p.Pro224Arg
NM_001271044.3:c.470C>G	NP_001257973.1:p.Pro157Arg
NM_001365902.2:c.494C>G	NP_001352831.1:p.Pro165Arg
NM_001365982.2:c.494C>G	NP_001352911.1:p.Pro165Arg
NM_001365983.2:c.353C>G	NP_001352912.1:p.Pro118Arg
NM_001365984.2:c.491C>G	NP_001352913.1:p.Pro164Arg
NM_001365985.2:c.491C>G	NP_001352914.1:p.Pro164Arg
NM_002501.4:c.494C>G	NP_002492.2:p.Pro165Arg
NM_001365902.3:c.494C>G MANE Select	NP_001352831.1:p.Pro165Arg
NM_001378404.1:c.470C>G	NP_001365333.1:p.Pro157Arg
NM_001378405.1:c.542C>G	NP_001365334.1:p.Pro181Arg