Canonical Allele Identifier: CA305547055

Gene: NFIX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13023687A>T , CM000681.2:g.13023687A>T	GRCh38
NC_000019.9:g.13134501A>T , CM000681.1:g.13134501A>T	GRCh37
NC_000019.8:g.12995501A>T	NCBI36
NG_032925.2:g.32918A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001365902.3:c.28-1334A>T MANE Select	NP_001352831.1:n.28-1334A>T
ENST00000592199.6:c.28-1334A>T MANE Select	ENSP00000467512.1:n.28-1334A>T
NM_001365902.1:c.28-1334A>T	NP_001352831.1:n.28-1334A>T
NM_001365902.2:c.28-1334A>T	NP_001352831.1:n.28-1334A>T
NM_001365982.1:c.28-1334A>T	NP_001352911.1:n.28-1334A>T
NM_001365982.2:c.28-1334A>T	NP_001352911.1:n.28-1334A>T
NM_002501.3:c.28-1334A>T	NP_002492.2:n.28-1334A>T
NM_002501.4:c.28-1334A>T	NP_002492.2:n.28-1334A>T
ENST00000397661.6:c.28-1334A>T	ENSP00000380781.2:n.28-1334A>T
ENST00000585382.5:c.-114-1334A>T	ENSP00000466605.1:n.-114-1334A>T
ENST00000590027.1:c.-114-1334A>T	ENSP00000465616.1:n.-114-1334A>T
ENST00000592199.5:c.28-1334A>T	ENSP00000467512.1:n.28-1334A>T
XM_005259918.3:c.28-1334A>T	XP_005259975.1:n.28-1334A>T
XM_005259920.3:c.-345A>T	XP_005259977.1:n.-345A>T