Canonical Allele Identifier: CA5120066

Gene: NFIL3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91409965T>G , CM000671.2:g.91409965T>G	GRCh38
NC_000009.11:g.94172247T>G , CM000671.1:g.94172247T>G	GRCh37
NC_000009.10:g.93212068T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005384.3:c.770A>C MANE Select	NP_005375.2:p.His257Pro
ENST00000297689.4:c.770A>C MANE Select	ENSP00000297689.2:p.His257Pro
NM_001289999.1:c.770A>C	NP_001276928.1:p.His257Pro
NM_001289999.2:c.770A>C	NP_001276928.1:p.His257Pro
NM_001290000.1:c.770A>C	NP_001276929.1:p.His257Pro
NM_001290000.2:c.770A>C	NP_001276929.1:p.His257Pro
NM_005384.2:c.770A>C	NP_005375.2:p.His257Pro
ENST00000297689.3:c.770A>C	ENSP00000297689.2:p.His257Pro
XM_017014743.1:c.770A>C	XP_016870232.1:p.His257Pro
XM_017014744.1:c.770A>C	XP_016870233.1:p.His257Pro