Canonical Allele Identifier: CA1619206245

Gene: NFKBIL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31557671C= , CM000668.2:g.31557671C=	GRCh38
NC_000006.11:g.31525448C= , CM000668.1:g.31525448C=	GRCh37
NC_000006.10:g.31633427C=	NCBI36
NG_012344.1:g.15821C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005007.4:c.378C= MANE Select	NP_004998.3:p.Ser126=
ENST00000376148.9:c.378C= MANE Select	ENSP00000365318.4:p.Ser126=
NM_001144961.1:c.378C=	NP_001138433.1:p.Ser126=
NM_001144961.2:c.378C=	NP_001138433.1:p.Ser126=
NM_001144962.1:c.309C=	NP_001138434.1:p.Ser103=
NM_001144962.2:c.309C=	NP_001138434.1:p.Ser103=
NM_001144963.1:c.309C=	NP_001138435.1:p.Ser103=
NM_001144963.2:c.309C=	NP_001138435.1:p.Ser103=
NM_005007.3:c.378C=	NP_004998.3:p.Ser126=
ENST00000376145.8:c.378C=	ENSP00000365315.4:p.Ser126=
ENST00000376146.8:c.309C=	ENSP00000365316.4:p.Ser103=
ENST00000376148.8:c.378C=	ENSP00000365318.4:p.Ser126=
ENST00000473655.1:n.412C=
ENST00000496233.1:c.*87C=	ENSP00000437148.1:n.*87C=
XR_926695.1:n.117-7112G=