Canonical Allele Identifier: CA505651474

Gene: NFIX

Linked Data

• MyVariant Identifiers: chr19:g.13192561G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13081747G>C , CM000681.2:g.13081747G>C	GRCh38
NC_000019.9:g.13192561G>C , CM000681.1:g.13192561G>C	GRCh37
NC_000019.8:g.13053561G>C	NCBI36
NG_032925.2:g.90978G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358552.8:c.1020G>C	ENSP00000351354.5:p.Pro340=
ENST00000622520.2:c.1075+3012G>C	ENSP00000481181.2:n.1075+3012G>C
ENST00000693124.1:c.773+6076G>C
ENST00000592199.6:c.1146G>C MANE Select	ENSP00000467512.1:p.Pro382=
ENST00000676441.1:c.1170G>C	ENSP00000502554.1:p.Pro390=
ENST00000358552.7:c.1032G>C	ENSP00000351354.4:p.Pro344=
ENST00000360105.8:c.1032G>C	ENSP00000353219.4:p.Pro344=
ENST00000397661.6:c.1146G>C	ENSP00000380781.2:p.Pro382=
ENST00000585382.5:c.*515G>C	ENSP00000466605.1:n.*515G>C
ENST00000585575.5:c.1122G>C	ENSP00000468794.1:p.Pro374=
ENST00000586797.5:c.*977G>C	ENSP00000467536.1:n.*977G>C
ENST00000587260.1:c.1143G>C	ENSP00000467785.1:p.Pro381=
ENST00000587760.5:c.1122G>C	ENSP00000466389.1:p.Pro374=
ENST00000588228.5:c.1005G>C	ENSP00000466735.1:p.Pro335=
ENST00000592199.5:c.1146G>C	ENSP00000467512.1:p.Pro382=
NM_001271043.2:c.1170G>C	NP_001257972.1:p.Pro390=
NM_001271044.2:c.1122G>C	NP_001257973.1:p.Pro374=
NM_002501.3:c.1146G>C	NP_002492.2:p.Pro382=
XM_005259917.3:c.1200G>C	XP_005259974.1:p.Pro400=
XM_005259918.3:c.1146G>C	XP_005259975.1:p.Pro382=
XM_005259919.3:c.1323G>C	XP_005259976.1:p.Pro441=
XM_005259920.3:c.1122G>C	XP_005259977.1:p.Pro374=
XM_005259921.3:c.1255+3012G>C	XP_005259978.1:n.1255+3012G>C
XM_005259922.3:c.1132+6076G>C	XP_005259979.1:n.1132+6076G>C
XM_006722760.2:c.1200G>C	XP_006722823.1:p.Pro400=
XM_011528040.1:c.1194G>C	XP_011526342.1:p.Pro398=
NM_001365902.1:c.1146G>C	NP_001352831.1:p.Pro382=
NM_001365982.1:c.1023G>C	NP_001352911.1:p.Pro341=
NM_001365983.1:c.1005G>C	NP_001352912.1:p.Pro335=
NM_001365984.1:c.1143G>C	NP_001352913.1:p.Pro381=
NM_001365985.1:c.1143G>C	NP_001352914.1:p.Pro381=
XM_005259917.4:c.1200G>C	XP_005259974.1:p.Pro400=
NM_001271044.3:c.1122G>C	NP_001257973.1:p.Pro374=
NM_001365902.2:c.1146G>C	NP_001352831.1:p.Pro382=
NM_001365982.2:c.1023G>C	NP_001352911.1:p.Pro341=
NM_001365983.2:c.1005G>C	NP_001352912.1:p.Pro335=
NM_001365984.2:c.1143G>C	NP_001352913.1:p.Pro381=
NM_001365985.2:c.1143G>C	NP_001352914.1:p.Pro381=
NM_002501.4:c.1146G>C	NP_002492.2:p.Pro382=
NM_001365902.3:c.1146G>C MANE Select	NP_001352831.1:p.Pro382=
NM_001378404.1:c.1122G>C	NP_001365333.1:p.Pro374=
NM_001378405.1:c.1194G>C	NP_001365334.1:p.Pro398=