Canonical Allele Identifier: CA9237138

Gene: NFIX

Linked Data

• dbSNP Id: rs771310547
• ExAC: 19:13192502 C / G
• gnomAD v2: 19-13192502-C-G
• gnomAD v3: 19-13081688-C-G
• gnomAD v4: 19-13081688-C-G
• MyVariant Identifiers: chr19:g.13192502C>G (hg19) ; chr19:g.13081688C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081688C>G , CM000681.2:g.13081688C>G	GRCh38
NC_000019.9:g.13192502C>G , CM000681.1:g.13192502C>G	GRCh37
NC_000019.8:g.13053502C>G	NCBI36
NG_032925.2:g.90919C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358552.8:c.961C>G	ENSP00000351354.5:p.Arg321Gly
ENST00000622520.2:c.1075+2953C>G	ENSP00000481181.2:n.1075+2953C>G
ENST00000693124.1:c.773+6017C>G
ENST00000592199.6:c.1087C>G MANE Select	ENSP00000467512.1:p.Arg363Gly
ENST00000676441.1:c.1111C>G	ENSP00000502554.1:p.Arg371Gly
ENST00000358552.7:c.973C>G	ENSP00000351354.4:p.Arg325Gly
ENST00000360105.8:c.973C>G	ENSP00000353219.4:p.Arg325Gly
ENST00000397661.6:c.1087C>G	ENSP00000380781.2:p.Arg363Gly
ENST00000585382.5:c.*456C>G	ENSP00000466605.1:n.*456C>G
ENST00000585575.5:c.1063C>G	ENSP00000468794.1:p.Arg355Gly
ENST00000586797.5:c.*918C>G	ENSP00000467536.1:n.*918C>G
ENST00000587260.1:c.1084C>G	ENSP00000467785.1:p.Arg362Gly
ENST00000587760.5:c.1063C>G	ENSP00000466389.1:p.Arg355Gly
ENST00000588228.5:c.946C>G	ENSP00000466735.1:p.Arg316Gly
ENST00000592199.5:c.1087C>G	ENSP00000467512.1:p.Arg363Gly
NM_001271043.2:c.1111C>G	NP_001257972.1:p.Arg371Gly
NM_001271044.2:c.1063C>G	NP_001257973.1:p.Arg355Gly
NM_002501.3:c.1087C>G	NP_002492.2:p.Arg363Gly
XM_005259917.3:c.1141C>G	XP_005259974.1:p.Arg381Gly
XM_005259918.3:c.1087C>G	XP_005259975.1:p.Arg363Gly
XM_005259919.3:c.1264C>G	XP_005259976.1:p.Arg422Gly
XM_005259920.3:c.1063C>G	XP_005259977.1:p.Arg355Gly
XM_005259921.3:c.1255+2953C>G	XP_005259978.1:n.1255+2953C>G
XM_005259922.3:c.1132+6017C>G	XP_005259979.1:n.1132+6017C>G
XM_006722760.2:c.1141C>G	XP_006722823.1:p.Arg381Gly
XM_011528040.1:c.1135C>G	XP_011526342.1:p.Arg379Gly
NM_001365902.1:c.1087C>G	NP_001352831.1:p.Arg363Gly
NM_001365982.1:c.964C>G	NP_001352911.1:p.Arg322Gly
NM_001365983.1:c.946C>G	NP_001352912.1:p.Arg316Gly
NM_001365984.1:c.1084C>G	NP_001352913.1:p.Arg362Gly
NM_001365985.1:c.1084C>G	NP_001352914.1:p.Arg362Gly
XM_005259917.4:c.1141C>G	XP_005259974.1:p.Arg381Gly
NM_001271044.3:c.1063C>G	NP_001257973.1:p.Arg355Gly
NM_001365902.2:c.1087C>G	NP_001352831.1:p.Arg363Gly
NM_001365982.2:c.964C>G	NP_001352911.1:p.Arg322Gly
NM_001365983.2:c.946C>G	NP_001352912.1:p.Arg316Gly
NM_001365984.2:c.1084C>G	NP_001352913.1:p.Arg362Gly
NM_001365985.2:c.1084C>G	NP_001352914.1:p.Arg362Gly
NM_002501.4:c.1087C>G	NP_002492.2:p.Arg363Gly
NM_001365902.3:c.1087C>G MANE Select	NP_001352831.1:p.Arg363Gly
NM_001378404.1:c.1063C>G	NP_001365333.1:p.Arg355Gly
NM_001378405.1:c.1135C>G	NP_001365334.1:p.Arg379Gly