Canonical Allele Identifier: CA1481441040

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102582695_102582696delinsGA , CM000666.2:g.102582695_102582696delinsGA	GRCh38
NC_000004.11:g.103503852_103503853delinsGA , CM000666.1:g.103503852_103503853delinsGA	GRCh37
NC_000004.10:g.103722890_103722891delinsGA	NCBI36
NG_050628.1:g.86367_86368delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.860-171_860-170delinsGA	ENSP00000426147.2:n.860-171_860-170delinsGA
ENST00000509165.2:c.836-171_836-170delinsGA	ENSP00000423877.2:n.836-171_836-170delinsGA
ENST00000697794.1:c.*477-171_*477-170delinsGA	ENSP00000513443.1:n.*477-171_*477-170delinsGA
ENST00000697799.1:n.333-171_333-170delinsGA
ENST00000697800.1:n.47-171_47-170delinsGA
ENST00000226574.9:c.836-171_836-170delinsGA MANE Select	ENSP00000226574.4:n.836-171_836-170delinsGA
ENST00000652569.1:c.811+61_811+62delinsGA
ENST00000652619.1:c.857-171_857-170delinsGA	ENSP00000499031.1:n.857-171_857-170delinsGA
ENST00000226574.8:c.836-171_836-170delinsGA	ENSP00000226574.4:n.836-171_836-170delinsGA
ENST00000394820.8:c.833-171_833-170delinsGA	ENSP00000378297.4:n.833-171_833-170delinsGA
ENST00000505458.5:c.833-171_833-170delinsGA	ENSP00000424790.1:n.833-171_833-170delinsGA
ENST00000508584.1:c.215-171_215-170delinsGA	ENSP00000424815.1:n.215-171_215-170delinsGA
ENST00000600343.5:c.293-171_293-170delinsGA	ENSP00000469340.1:n.293-171_293-170delinsGA
NM_001165412.1:c.833-171_833-170delinsGA	NP_001158884.1:n.833-171_833-170delinsGA
NM_003998.3:c.836-171_836-170delinsGA	NP_003989.2:n.836-171_836-170delinsGA
XM_011532006.1:c.857-171_857-170delinsGA	XP_011530308.1:n.857-171_857-170delinsGA
XM_011532007.1:c.833-171_833-170delinsGA	XP_011530309.1:n.833-171_833-170delinsGA
XM_011532008.1:c.677-171_677-170delinsGA	XP_011530310.1:n.677-171_677-170delinsGA
XM_011532009.1:c.440-171_440-170delinsGA	XP_011530311.1:n.440-171_440-170delinsGA
NM_001319226.1:c.833-171_833-170delinsGA	NP_001306155.1:n.833-171_833-170delinsGA
XM_011532006.2:c.857-171_857-170delinsGA	XP_011530308.1:n.857-171_857-170delinsGA
XM_024454067.1:c.860-171_860-170delinsGA	XP_024309835.1:n.860-171_860-170delinsGA
XM_024454068.1:c.836-171_836-170delinsGA	XP_024309836.1:n.836-171_836-170delinsGA
XM_024454069.1:c.701-171_701-170delinsGA	XP_024309837.1:n.701-171_701-170delinsGA
NM_003998.4:c.836-171_836-170delinsGA MANE Select	NP_003989.2:n.836-171_836-170delinsGA
NM_001165412.2:c.833-171_833-170delinsGA	NP_001158884.1:n.833-171_833-170delinsGA
NM_001319226.2:c.833-171_833-170delinsGA	NP_001306155.1:n.833-171_833-170delinsGA
NM_001382625.1:c.836-171_836-170delinsGA	NP_001369554.1:n.836-171_836-170delinsGA
NM_001382626.1:c.836-171_836-170delinsGA	NP_001369555.1:n.836-171_836-170delinsGA
NM_001382627.1:c.833-171_833-170delinsGA	NP_001369556.1:n.833-171_833-170delinsGA
NM_001382628.1:c.794-171_794-170delinsGA	NP_001369557.1:n.794-171_794-170delinsGA