Canonical Allele Identifier: CA404312419

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13025034C>G , CM000681.2:g.13025034C>G	GRCh38
NC_000019.9:g.13135848C>G , CM000681.1:g.13135848C>G	GRCh37
NC_000019.8:g.12996848C>G	NCBI36
NG_032925.2:g.34265C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365902.3:c.41C>G MANE Select	NP_001352831.1:p.Pro14Arg
ENST00000592199.6:c.41C>G MANE Select	ENSP00000467512.1:p.Pro14Arg
NM_001271043.2:c.65C>G	NP_001257972.1:p.Pro22Arg
NM_001271044.2:c.17C>G	NP_001257973.1:p.Pro6Arg
NM_001271044.3:c.17C>G	NP_001257973.1:p.Pro6Arg
NM_001365902.1:c.41C>G	NP_001352831.1:p.Pro14Arg
NM_001365902.2:c.41C>G	NP_001352831.1:p.Pro14Arg
NM_001365982.1:c.41C>G	NP_001352911.1:p.Pro14Arg
NM_001365982.2:c.41C>G	NP_001352911.1:p.Pro14Arg
NM_001365983.1:c.-101C>G	NP_001352912.1:n.-101C>G
NM_001365983.2:c.-101C>G	NP_001352912.1:n.-101C>G
NM_001365984.1:c.38C>G	NP_001352913.1:p.Pro13Arg
NM_001365984.2:c.38C>G	NP_001352913.1:p.Pro13Arg
NM_001365985.1:c.38C>G	NP_001352914.1:p.Pro13Arg
NM_001365985.2:c.38C>G	NP_001352914.1:p.Pro13Arg
NM_001378404.1:c.17C>G	NP_001365333.1:p.Pro6Arg
NM_001378405.1:c.89C>G	NP_001365334.1:p.Pro30Arg
NM_002501.3:c.41C>G	NP_002492.2:p.Pro14Arg
NM_002501.4:c.41C>G	NP_002492.2:p.Pro14Arg
ENST00000358552.7:c.50C>G	ENSP00000351354.4:p.Pro17Arg
ENST00000358552.8:c.38C>G	ENSP00000351354.5:p.Pro13Arg
ENST00000360105.8:c.50C>G	ENSP00000353219.4:p.Pro17Arg
ENST00000397661.6:c.41C>G	ENSP00000380781.2:p.Pro14Arg
ENST00000585382.5:c.-101C>G	ENSP00000466605.1:n.-101C>G
ENST00000585575.5:c.17C>G	ENSP00000468794.1:p.Pro6Arg
ENST00000586797.5:c.52C>G	ENSP00000467536.1:p.Arg18Gly
ENST00000586873.1:c.-101C>G	ENSP00000468707.1:n.-101C>G
ENST00000587260.1:c.38C>G	ENSP00000467785.1:p.Pro13Arg
ENST00000587760.5:c.17C>G	ENSP00000466389.1:p.Pro6Arg
ENST00000588228.5:c.-101C>G	ENSP00000466735.1:n.-101C>G
ENST00000590027.1:c.-101C>G	ENSP00000465616.1:n.-101C>G
ENST00000591028.1:c.89C>G	ENSP00000465094.1:p.Pro30Arg
ENST00000592199.5:c.41C>G	ENSP00000467512.1:p.Pro14Arg
ENST00000622520.2:c.38C>G	ENSP00000481181.2:p.Pro13Arg
ENST00000676441.1:c.65C>G	ENSP00000502554.1:p.Pro22Arg
XM_005259917.3:c.218C>G	XP_005259974.1:p.Pro73Arg
XM_005259917.4:c.218C>G	XP_005259974.1:p.Pro73Arg
XM_005259918.3:c.41C>G	XP_005259975.1:p.Pro14Arg
XM_005259919.3:c.218C>G	XP_005259976.1:p.Pro73Arg
XM_005259920.3:c.17C>G	XP_005259977.1:p.Pro6Arg
XM_005259921.3:c.218C>G	XP_005259978.1:p.Pro73Arg
XM_005259922.3:c.218C>G	XP_005259979.1:p.Pro73Arg
XM_006722760.2:c.218C>G	XP_006722823.1:p.Pro73Arg
XM_011528040.1:c.89C>G	XP_011526342.1:p.Pro30Arg