Canonical Allele Identifier: CA1481415273

Gene: NFKB1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102513096T>G , CM000666.2:g.102513096T>G	GRCh38
NC_000004.11:g.103434253T>G , CM000666.1:g.103434253T>G	GRCh37
NC_000004.10:g.103653283T>G	NCBI36
NG_050628.1:g.16768T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.17+2147T>G	ENSP00000426147.2:n.17+2147T>G
ENST00000509165.2:c.-8+9606T>G	ENSP00000423877.2:n.-8+9606T>G
ENST00000697793.1:n.178+11308T>G
ENST00000697794.1:c.-8+11308T>G	ENSP00000513443.1:n.-8+11308T>G
ENST00000697795.1:n.46+11308T>G
ENST00000697796.1:n.275+10924T>G
ENST00000697797.1:n.196+10924T>G
ENST00000226574.9:c.-8+11308T>G MANE Select	ENSP00000226574.4:n.-8+11308T>G
ENST00000652619.1:c.17+2147T>G	ENSP00000499031.1:n.17+2147T>G
ENST00000226574.8:c.-8+11308T>G	ENSP00000226574.4:n.-8+11308T>G
ENST00000394820.8:c.-8+11308T>G	ENSP00000378297.4:n.-8+11308T>G
ENST00000505458.5:c.-8+10929T>G	ENSP00000424790.1:n.-8+10929T>G
ENST00000507079.5:c.17+2147T>G	ENSP00000426147.1:n.17+2147T>G
ENST00000509165.1:c.-8+9606T>G	ENSP00000423877.1:n.-8+9606T>G
ENST00000511926.5:c.17+2147T>G	ENSP00000420904.1:n.17+2147T>G
NM_001165412.1:c.-8+11308T>G	NP_001158884.1:n.-8+11308T>G
NM_003998.3:c.-8+11308T>G	NP_003989.2:n.-8+11308T>G
XM_011532006.1:c.17+2147T>G	XP_011530308.1:n.17+2147T>G
XM_011532007.1:c.-8+10929T>G	XP_011530309.1:n.-8+10929T>G
NM_001319226.1:c.-8+10929T>G	NP_001306155.1:n.-8+10929T>G
XM_011532006.2:c.17+2147T>G	XP_011530308.1:n.17+2147T>G
XM_024454067.1:c.17+2147T>G	XP_024309835.1:n.17+2147T>G
XM_024454069.1:c.17+2147T>G	XP_024309837.1:n.17+2147T>G
NM_003998.4:c.-8+11308T>G MANE Select	NP_003989.2:n.-8+11308T>G
NM_001165412.2:c.-8+11308T>G	NP_001158884.1:n.-8+11308T>G
NM_001319226.2:c.-8+10929T>G	NP_001306155.1:n.-8+10929T>G
NM_001382625.1:c.-8+2147T>G	NP_001369554.1:n.-8+2147T>G
NM_001382626.1:c.-8+2147T>G	NP_001369555.1:n.-8+2147T>G
NM_001382627.1:c.-8+2147T>G	NP_001369556.1:n.-8+2147T>G
NM_001382628.1:c.-1+11308T>G	NP_001369557.1:n.-1+11308T>G