Canonical Allele Identifier: CA505780779

Gene: NFIX

Linked Data

• gnomAD v4: 19-13025377-G-T
• MyVariant Identifiers: chr19:g.13136191G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13025377G>T , CM000681.2:g.13025377G>T	GRCh38
NC_000019.9:g.13136191G>T , CM000681.1:g.13136191G>T	GRCh37
NC_000019.8:g.12997191G>T	NCBI36
NG_032925.2:g.34608G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358552.8:c.381G>T	ENSP00000351354.5:p.Arg127=
ENST00000622520.2:c.381G>T	ENSP00000481181.2:p.Arg127=
ENST00000693124.1:c.202G>T
ENST00000592199.6:c.384G>T MANE Select	ENSP00000467512.1:p.Arg128=
ENST00000676441.1:c.408G>T	ENSP00000502554.1:p.Arg136=
ENST00000358552.7:c.393G>T	ENSP00000351354.4:p.Arg131=
ENST00000360105.8:c.393G>T	ENSP00000353219.4:p.Arg131=
ENST00000397661.6:c.384G>T	ENSP00000380781.2:p.Arg128=
ENST00000585382.5:c.234+9G>T	ENSP00000466605.1:n.234+9G>T
ENST00000585575.5:c.360G>T	ENSP00000468794.1:p.Arg120=
ENST00000586797.5:c.*215G>T	ENSP00000467536.1:n.*215G>T
ENST00000586873.1:c.243G>T	ENSP00000468707.1:p.Arg81=
ENST00000587260.1:c.381G>T	ENSP00000467785.1:p.Arg127=
ENST00000587760.5:c.360G>T	ENSP00000466389.1:p.Arg120=
ENST00000588228.5:c.243G>T	ENSP00000466735.1:p.Arg81=
ENST00000590027.1:c.243G>T	ENSP00000465616.1:p.Arg81=
ENST00000591028.1:c.432G>T	ENSP00000465094.1:p.Arg144=
ENST00000592199.5:c.384G>T	ENSP00000467512.1:p.Arg128=
NM_001271043.2:c.408G>T	NP_001257972.1:p.Arg136=
NM_001271044.2:c.360G>T	NP_001257973.1:p.Arg120=
NM_002501.3:c.384G>T	NP_002492.2:p.Arg128=
XM_005259917.3:c.561G>T	XP_005259974.1:p.Arg187=
XM_005259918.3:c.384G>T	XP_005259975.1:p.Arg128=
XM_005259919.3:c.561G>T	XP_005259976.1:p.Arg187=
XM_005259920.3:c.360G>T	XP_005259977.1:p.Arg120=
XM_005259921.3:c.561G>T	XP_005259978.1:p.Arg187=
XM_005259922.3:c.561G>T	XP_005259979.1:p.Arg187=
XM_006722760.2:c.561G>T	XP_006722823.1:p.Arg187=
XM_011528040.1:c.432G>T	XP_011526342.1:p.Arg144=
NM_001365902.1:c.384G>T	NP_001352831.1:p.Arg128=
NM_001365982.1:c.384G>T	NP_001352911.1:p.Arg128=
NM_001365983.1:c.243G>T	NP_001352912.1:p.Arg81=
NM_001365984.1:c.381G>T	NP_001352913.1:p.Arg127=
NM_001365985.1:c.381G>T	NP_001352914.1:p.Arg127=
XM_005259917.4:c.561G>T	XP_005259974.1:p.Arg187=
NM_001271044.3:c.360G>T	NP_001257973.1:p.Arg120=
NM_001365902.2:c.384G>T	NP_001352831.1:p.Arg128=
NM_001365982.2:c.384G>T	NP_001352911.1:p.Arg128=
NM_001365983.2:c.243G>T	NP_001352912.1:p.Arg81=
NM_001365984.2:c.381G>T	NP_001352913.1:p.Arg127=
NM_001365985.2:c.381G>T	NP_001352914.1:p.Arg127=
NM_002501.4:c.384G>T	NP_002492.2:p.Arg128=
NM_001365902.3:c.384G>T MANE Select	NP_001352831.1:p.Arg128=
NM_001378404.1:c.360G>T	NP_001365333.1:p.Arg120=
NM_001378405.1:c.432G>T	NP_001365334.1:p.Arg144=