Canonical Allele Identifier: CA16618021
Gene: NFKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102578895C>G , CM000666.2:g.102578895C>G GRCh38
NC_000004.11:g.103500052C>G , CM000666.1:g.103500052C>G GRCh37
NC_000004.10:g.103719090C>G NCBI36
NG_050628.1:g.82567C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507079.6:c.610C>G ENSP00000426147.2:p.Leu204Val
ENST00000509165.2:c.586C>G ENSP00000423877.2:p.Leu196Val
ENST00000697793.1:n.684C>G
ENST00000697794.1:c.*227C>G ENSP00000513443.1:n.*227C>G
ENST00000226574.9:c.586C>G MANE Select ENSP00000226574.4:p.Leu196Val
ENST00000652569.1:c.500C>G
ENST00000652619.1:c.607C>G ENSP00000499031.1:p.Leu203Val
ENST00000226574.8:c.586C>G ENSP00000226574.4:p.Leu196Val
ENST00000394820.8:c.583C>G ENSP00000378297.4:p.Leu195Val
ENST00000505458.5:c.583C>G ENSP00000424790.1:p.Leu195Val
ENST00000508584.1:c.-36C>G ENSP00000424815.1:n.-36C>G
ENST00000510638.1:n.430C>G
ENST00000513803.5:n.469C>G
ENST00000600343.5:c.43C>G ENSP00000469340.1:p.Leu15Val
NM_001165412.1:c.583C>G NP_001158884.1:p.Leu195Val
NM_003998.3:c.586C>G NP_003989.2:p.Leu196Val
XM_011532006.1:c.607C>G XP_011530308.1:p.Leu203Val
XM_011532007.1:c.583C>G XP_011530309.1:p.Leu195Val
XM_011532008.1:c.572-1640C>G XP_011530310.1:n.572-1640C>G
XM_011532009.1:c.190C>G XP_011530311.1:p.Leu64Val
NM_001319226.1:c.583C>G NP_001306155.1:p.Leu195Val
XM_011532006.2:c.607C>G XP_011530308.1:p.Leu203Val
XM_024454067.1:c.610C>G XP_024309835.1:p.Leu204Val
XM_024454068.1:c.586C>G XP_024309836.1:p.Leu196Val
XM_024454069.1:c.596-1640C>G XP_024309837.1:n.596-1640C>G
NM_003998.4:c.586C>G MANE Select NP_003989.2:p.Leu196Val
NM_001165412.2:c.583C>G NP_001158884.1:p.Leu195Val
NM_001319226.2:c.583C>G NP_001306155.1:p.Leu195Val
NM_001382625.1:c.586C>G NP_001369554.1:p.Leu196Val
NM_001382626.1:c.586C>G NP_001369555.1:p.Leu196Val
NM_001382627.1:c.583C>G NP_001369556.1:p.Leu195Val
NM_001382628.1:c.544C>G NP_001369557.1:p.Leu182Val