Canonical Allele Identifier: CA2321543485

Gene: NFILZ

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8679464A= , CM000681.2:g.8679464A=	GRCh38
NC_000019.9:g.8789728A= , CM000681.1:g.8789728A=	GRCh37
NC_000019.8:g.8650728A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000570582.4:c.*1829A=	ENSP00000500121.1:n.*1829A=
ENST00000671902.2:c.*1829A=	ENSP00000500604.1:n.*1829A=
ENST00000673603.2:c.*1829A=	ENSP00000499970.1:n.*1829A=
ENST00000691075.1:c.*1829A= MANE Select	ENSP00000509575.1:n.*1829A=
NM_001378599.1:c.*1829A=	NP_001365528.1:n.*1829A=
NM_001378600.1:c.*1829A= MANE Select	NP_001365529.1:n.*1829A=
NM_001378601.1:c.*1829A=	NP_001365530.1:n.*1829A=