Canonical Allele Identifier: CA3026555
Gene: NFKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102616574C>T , CM000666.2:g.102616574C>T GRCh38
NC_000004.11:g.103537731C>T , CM000666.1:g.103537731C>T GRCh37
NC_000004.10:g.103756777C>T NCBI36
NG_050628.1:g.120246C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000507079.6:c.2914C>T ENSP00000426147.2:p.Pro972Ser
ENST00000509165.2:c.2890C>T ENSP00000423877.2:p.Pro964Ser
ENST00000697794.1:c.*2531C>T ENSP00000513443.1:n.*2531C>T
ENST00000697799.1:n.2387C>T
ENST00000697801.1:n.1091C>T
ENST00000698233.1:n.2619C>T
ENST00000226574.9:c.2890C>T MANE Select ENSP00000226574.4:p.Pro964Ser
ENST00000652569.1:c.2866C>T
ENST00000652619.1:c.*1417C>T ENSP00000499031.1:n.*1417C>T
ENST00000226574.8:c.2890C>T ENSP00000226574.4:p.Pro964Ser
ENST00000394820.8:c.2887C>T ENSP00000378297.4:p.Pro963Ser
ENST00000505458.5:c.2887C>T ENSP00000424790.1:p.Pro963Ser
ENST00000600343.5:c.2347C>T ENSP00000469340.1:p.Pro783Ser
NM_001165412.1:c.2887C>T NP_001158884.1:p.Pro963Ser
NM_003998.3:c.2890C>T NP_003989.2:p.Pro964Ser
XM_011532006.1:c.2911C>T XP_011530308.1:p.Pro971Ser
XM_011532007.1:c.2887C>T XP_011530309.1:p.Pro963Ser
XM_011532008.1:c.2731C>T XP_011530310.1:p.Pro911Ser
XM_011532009.1:c.2494C>T XP_011530311.1:p.Pro832Ser
NM_001319226.1:c.2887C>T NP_001306155.1:p.Pro963Ser
XM_011532006.2:c.2911C>T XP_011530308.1:p.Pro971Ser
XM_024454067.1:c.2914C>T XP_024309835.1:p.Pro972Ser
XM_024454068.1:c.2890C>T XP_024309836.1:p.Pro964Ser
XM_024454069.1:c.2755C>T XP_024309837.1:p.Pro919Ser
NM_003998.4:c.2890C>T MANE Select NP_003989.2:p.Pro964Ser
NM_001165412.2:c.2887C>T NP_001158884.1:p.Pro963Ser
NM_001319226.2:c.2887C>T NP_001306155.1:p.Pro963Ser
NM_001382625.1:c.2890C>T NP_001369554.1:p.Pro964Ser
NM_001382626.1:c.2890C>T NP_001369555.1:p.Pro964Ser
NM_001382627.1:c.2887C>T NP_001369556.1:p.Pro963Ser
NM_001382628.1:c.2848C>T NP_001369557.1:p.Pro950Ser