Canonical Allele Identifier: CA1619204093

Gene: NFKBIL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31552649C= , CM000668.2:g.31552649C=	GRCh38
NC_000006.11:g.31520426C= , CM000668.1:g.31520426C=	GRCh37
NC_000006.10:g.31628405C=	NCBI36
NG_012344.1:g.10799C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005007.4:c.334+4210C= MANE Select	NP_004998.3:n.334+4210C=
ENST00000376148.9:c.334+4210C= MANE Select	ENSP00000365318.4:n.334+4210C=
NM_001144961.1:c.334+4210C=	NP_001138433.1:n.334+4210C=
NM_001144961.2:c.334+4210C=	NP_001138433.1:n.334+4210C=
NM_001144962.1:c.265+4210C=	NP_001138434.1:n.265+4210C=
NM_001144962.2:c.265+4210C=	NP_001138434.1:n.265+4210C=
NM_001144963.1:c.265+4210C=	NP_001138435.1:n.265+4210C=
NM_001144963.2:c.265+4210C=	NP_001138435.1:n.265+4210C=
NM_005007.3:c.334+4210C=	NP_004998.3:n.334+4210C=
ENST00000376145.8:c.334+4210C=	ENSP00000365315.4:n.334+4210C=
ENST00000376146.8:c.265+4210C=	ENSP00000365316.4:n.265+4210C=
ENST00000376148.8:c.334+4210C=	ENSP00000365318.4:n.334+4210C=
ENST00000473655.1:n.368+4210C=
ENST00000496233.1:c.335-4048C=	ENSP00000437148.1:n.335-4048C=
XR_926695.1:n.117-2090G=