Canonical Allele Identifier: CA2508558544

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102598647_102598648insGTG , CM000666.2:g.102598647_102598648insGTG	GRCh38
NC_000004.11:g.103519804_103519805insGTG , CM000666.1:g.103519804_103519805insGTG	GRCh37
NC_000004.10:g.103738842_103738843insGTG	NCBI36
NG_050628.1:g.102319_102320insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.1661+986_1661+987insGTG	ENSP00000426147.2:n.1661+986_1661+987insGTG
ENST00000509165.2:c.1637+986_1637+987insGTG	ENSP00000423877.2:n.1637+986_1637+987insGTG
ENST00000697794.1:c.*1278+986_*1278+987insGTG	ENSP00000513443.1:n.*1278+986_*1278+987insGTG
ENST00000697799.1:n.1134+986_1134+987insGTG
ENST00000698233.1:n.1366+986_1366+987insGTG
ENST00000226574.9:c.1637+986_1637+987insGTG MANE Select	ENSP00000226574.4:n.1637+986_1637+987insGTG
ENST00000652569.1:c.1613+986_1613+987insGTG
ENST00000652619.1:c.*164+986_*164+987insGTG	ENSP00000499031.1:n.*164+986_*164+987insGTG
ENST00000226574.8:c.1637+986_1637+987insGTG	ENSP00000226574.4:n.1637+986_1637+987insGTG
ENST00000394820.8:c.1634+986_1634+987insGTG	ENSP00000378297.4:n.1634+986_1634+987insGTG
ENST00000505458.5:c.1634+986_1634+987insGTG	ENSP00000424790.1:n.1634+986_1634+987insGTG
ENST00000600343.5:c.1094+986_1094+987insGTG	ENSP00000469340.1:n.1094+986_1094+987insGTG
NM_001165412.1:c.1634+986_1634+987insGTG	NP_001158884.1:n.1634+986_1634+987insGTG
NM_003998.3:c.1637+986_1637+987insGTG	NP_003989.2:n.1637+986_1637+987insGTG
XM_011532006.1:c.1658+986_1658+987insGTG	XP_011530308.1:n.1658+986_1658+987insGTG
XM_011532007.1:c.1634+986_1634+987insGTG	XP_011530309.1:n.1634+986_1634+987insGTG
XM_011532008.1:c.1478+986_1478+987insGTG	XP_011530310.1:n.1478+986_1478+987insGTG
XM_011532009.1:c.1241+986_1241+987insGTG	XP_011530311.1:n.1241+986_1241+987insGTG
XR_939027.1:n.3679_3680insCAC
NM_001319226.1:c.1634+986_1634+987insGTG	NP_001306155.1:n.1634+986_1634+987insGTG
XM_011532006.2:c.1658+986_1658+987insGTG	XP_011530308.1:n.1658+986_1658+987insGTG
XM_024454067.1:c.1661+986_1661+987insGTG	XP_024309835.1:n.1661+986_1661+987insGTG
XM_024454068.1:c.1637+986_1637+987insGTG	XP_024309836.1:n.1637+986_1637+987insGTG
XM_024454069.1:c.1502+986_1502+987insGTG	XP_024309837.1:n.1502+986_1502+987insGTG
NM_003998.4:c.1637+986_1637+987insGTG MANE Select	NP_003989.2:n.1637+986_1637+987insGTG
NM_001165412.2:c.1634+986_1634+987insGTG	NP_001158884.1:n.1634+986_1634+987insGTG
NM_001319226.2:c.1634+986_1634+987insGTG	NP_001306155.1:n.1634+986_1634+987insGTG
NM_001382625.1:c.1637+986_1637+987insGTG	NP_001369554.1:n.1637+986_1637+987insGTG
NM_001382626.1:c.1637+986_1637+987insGTG	NP_001369555.1:n.1637+986_1637+987insGTG
NM_001382627.1:c.1634+986_1634+987insGTG	NP_001369556.1:n.1634+986_1634+987insGTG
NM_001382628.1:c.1595+986_1595+987insGTG	NP_001369557.1:n.1595+986_1595+987insGTG