Canonical Allele Identifier: CA2582789088

Gene: NFIX

Linked Data

• gnomAD v4: 19-13025577-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13025581_13025582del , CM000681.2:g.13025581_13025582del	GRCh38
NC_000019.9:g.13136395_13136396del , CM000681.1:g.13136395_13136396del	GRCh37
NC_000019.8:g.12997395_12997396del	NCBI36
NG_032925.2:g.34812_34813del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358552.8:c.556+29_556+30del	ENSP00000351354.5:n.556+29_556+30del
ENST00000622520.2:c.556+29_556+30del	ENSP00000481181.2:n.556+29_556+30del
ENST00000693124.1:c.377+29_377+30del
ENST00000592199.6:c.559+29_559+30del MANE Select	ENSP00000467512.1:n.559+29_559+30del
ENST00000676441.1:c.583+29_583+30del	ENSP00000502554.1:n.583+29_583+30del
ENST00000358552.7:c.568+29_568+30del	ENSP00000351354.4:n.568+29_568+30del
ENST00000360105.8:c.568+29_568+30del	ENSP00000353219.4:n.568+29_568+30del
ENST00000397661.6:c.559+29_559+30del	ENSP00000380781.2:n.559+29_559+30del
ENST00000585382.5:c.234+213_234+214del	ENSP00000466605.1:n.234+213_234+214del
ENST00000585575.5:c.535+29_535+30del	ENSP00000468794.1:n.535+29_535+30del
ENST00000586797.5:c.*390+29_*390+30del	ENSP00000467536.1:n.*390+29_*390+30del
ENST00000587260.1:c.556+29_556+30del	ENSP00000467785.1:n.556+29_556+30del
ENST00000587760.5:c.535+29_535+30del	ENSP00000466389.1:n.535+29_535+30del
ENST00000588228.5:c.418+29_418+30del	ENSP00000466735.1:n.418+29_418+30del
ENST00000592199.5:c.559+29_559+30del	ENSP00000467512.1:n.559+29_559+30del
NM_001271043.2:c.583+29_583+30del	NP_001257972.1:n.583+29_583+30del
NM_001271044.2:c.535+29_535+30del	NP_001257973.1:n.535+29_535+30del
NM_002501.3:c.559+29_559+30del	NP_002492.2:n.559+29_559+30del
XM_005259917.3:c.736+29_736+30del	XP_005259974.1:n.736+29_736+30del
XM_005259918.3:c.559+29_559+30del	XP_005259975.1:n.559+29_559+30del
XM_005259919.3:c.736+29_736+30del	XP_005259976.1:n.736+29_736+30del
XM_005259920.3:c.535+29_535+30del	XP_005259977.1:n.535+29_535+30del
XM_005259921.3:c.736+29_736+30del	XP_005259978.1:n.736+29_736+30del
XM_005259922.3:c.736+29_736+30del	XP_005259979.1:n.736+29_736+30del
XM_006722760.2:c.736+29_736+30del	XP_006722823.1:n.736+29_736+30del
XM_011528040.1:c.607+29_607+30del	XP_011526342.1:n.607+29_607+30del
NM_001365902.1:c.559+29_559+30del	NP_001352831.1:n.559+29_559+30del
NM_001365982.1:c.559+29_559+30del	NP_001352911.1:n.559+29_559+30del
NM_001365983.1:c.418+29_418+30del	NP_001352912.1:n.418+29_418+30del
NM_001365984.1:c.556+29_556+30del	NP_001352913.1:n.556+29_556+30del
NM_001365985.1:c.556+29_556+30del	NP_001352914.1:n.556+29_556+30del
XM_005259917.4:c.736+29_736+30del	XP_005259974.1:n.736+29_736+30del
NM_001271044.3:c.535+29_535+30del	NP_001257973.1:n.535+29_535+30del
NM_001365902.2:c.559+29_559+30del	NP_001352831.1:n.559+29_559+30del
NM_001365982.2:c.559+29_559+30del	NP_001352911.1:n.559+29_559+30del
NM_001365983.2:c.418+29_418+30del	NP_001352912.1:n.418+29_418+30del
NM_001365984.2:c.556+29_556+30del	NP_001352913.1:n.556+29_556+30del
NM_001365985.2:c.556+29_556+30del	NP_001352914.1:n.556+29_556+30del
NM_002501.4:c.559+29_559+30del	NP_002492.2:n.559+29_559+30del
NM_001365902.3:c.559+29_559+30del MANE Select	NP_001352831.1:n.559+29_559+30del
NM_001378404.1:c.535+29_535+30del	NP_001365333.1:n.535+29_535+30del
NM_001378405.1:c.607+29_607+30del	NP_001365334.1:n.607+29_607+30del