Canonical Allele Identifier: CA1481447776
Gene: NFKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102598563_102598574delinsATGTGGTATAAC , CM000666.2:g.102598563_102598574delinsATGTGGTATAAC GRCh38
NC_000004.11:g.103519720_103519731delinsATGTGGTATAAC , CM000666.1:g.103519720_103519731delinsATGTGGTATAAC GRCh37
NC_000004.10:g.103738758_103738769delinsATGTGGTATAAC NCBI36
NG_050628.1:g.102235_102246delinsATGTGGTATAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000507079.6:c.1661+902_1661+913delinsATGTGGTATAAC ENSP00000426147.2:n.1661+902_1661+913delinsATGTGGTATAAC
ENST00000509165.2:c.1637+902_1637+913delinsATGTGGTATAAC ENSP00000423877.2:n.1637+902_1637+913delinsATGTGGTATAAC
ENST00000697794.1:c.*1278+902_*1278+913delinsATGTGGTATAAC ENSP00000513443.1:n.*1278+902_*1278+913delinsATGTGGTATAAC
ENST00000697799.1:n.1134+902_1134+913delinsATGTGGTATAAC
ENST00000698233.1:n.1366+902_1366+913delinsATGTGGTATAAC
ENST00000226574.9:c.1637+902_1637+913delinsATGTGGTATAAC MANE Select ENSP00000226574.4:n.1637+902_1637+913delinsATGTGGTATAAC
ENST00000652569.1:c.1613+902_1613+913delinsATGTGGTATAAC
ENST00000652619.1:c.*164+902_*164+913delinsATGTGGTATAAC ENSP00000499031.1:n.*164+902_*164+913delinsATGTGGTATAAC
ENST00000226574.8:c.1637+902_1637+913delinsATGTGGTATAAC ENSP00000226574.4:n.1637+902_1637+913delinsATGTGGTATAAC
ENST00000394820.8:c.1634+902_1634+913delinsATGTGGTATAAC ENSP00000378297.4:n.1634+902_1634+913delinsATGTGGTATAAC
ENST00000505458.5:c.1634+902_1634+913delinsATGTGGTATAAC ENSP00000424790.1:n.1634+902_1634+913delinsATGTGGTATAAC
ENST00000600343.5:c.1094+902_1094+913delinsATGTGGTATAAC ENSP00000469340.1:n.1094+902_1094+913delinsATGTGGTATAAC
NM_001165412.1:c.1634+902_1634+913delinsATGTGGTATAAC NP_001158884.1:n.1634+902_1634+913delinsATGTGGTATAAC
NM_003998.3:c.1637+902_1637+913delinsATGTGGTATAAC NP_003989.2:n.1637+902_1637+913delinsATGTGGTATAAC
XM_011532006.1:c.1658+902_1658+913delinsATGTGGTATAAC XP_011530308.1:n.1658+902_1658+913delinsATGTGGTATAAC
XM_011532007.1:c.1634+902_1634+913delinsATGTGGTATAAC XP_011530309.1:n.1634+902_1634+913delinsATGTGGTATAAC
XM_011532008.1:c.1478+902_1478+913delinsATGTGGTATAAC XP_011530310.1:n.1478+902_1478+913delinsATGTGGTATAAC
XM_011532009.1:c.1241+902_1241+913delinsATGTGGTATAAC XP_011530311.1:n.1241+902_1241+913delinsATGTGGTATAAC
XR_939027.1:n.3753_3764delinsGTTATACCACAT
NM_001319226.1:c.1634+902_1634+913delinsATGTGGTATAAC NP_001306155.1:n.1634+902_1634+913delinsATGTGGTATAAC
XM_011532006.2:c.1658+902_1658+913delinsATGTGGTATAAC XP_011530308.1:n.1658+902_1658+913delinsATGTGGTATAAC
XM_024454067.1:c.1661+902_1661+913delinsATGTGGTATAAC XP_024309835.1:n.1661+902_1661+913delinsATGTGGTATAAC
XM_024454068.1:c.1637+902_1637+913delinsATGTGGTATAAC XP_024309836.1:n.1637+902_1637+913delinsATGTGGTATAAC
XM_024454069.1:c.1502+902_1502+913delinsATGTGGTATAAC XP_024309837.1:n.1502+902_1502+913delinsATGTGGTATAAC
NM_003998.4:c.1637+902_1637+913delinsATGTGGTATAAC MANE Select NP_003989.2:n.1637+902_1637+913delinsATGTGGTATAAC
NM_001165412.2:c.1634+902_1634+913delinsATGTGGTATAAC NP_001158884.1:n.1634+902_1634+913delinsATGTGGTATAAC
NM_001319226.2:c.1634+902_1634+913delinsATGTGGTATAAC NP_001306155.1:n.1634+902_1634+913delinsATGTGGTATAAC
NM_001382625.1:c.1637+902_1637+913delinsATGTGGTATAAC NP_001369554.1:n.1637+902_1637+913delinsATGTGGTATAAC
NM_001382626.1:c.1637+902_1637+913delinsATGTGGTATAAC NP_001369555.1:n.1637+902_1637+913delinsATGTGGTATAAC
NM_001382627.1:c.1634+902_1634+913delinsATGTGGTATAAC NP_001369556.1:n.1634+902_1634+913delinsATGTGGTATAAC
NM_001382628.1:c.1595+902_1595+913delinsATGTGGTATAAC NP_001369557.1:n.1595+902_1595+913delinsATGTGGTATAAC