Canonical Allele Identifier: CA1481447714

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102598426_102598427delinsCT , CM000666.2:g.102598426_102598427delinsCT	GRCh38
NC_000004.11:g.103519583_103519584delinsCT , CM000666.1:g.103519583_103519584delinsCT	GRCh37
NC_000004.10:g.103738621_103738622delinsCT	NCBI36
NG_050628.1:g.102098_102099delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.1661+765_1661+766delinsCT	ENSP00000426147.2:n.1661+765_1661+766delinsCT
ENST00000509165.2:c.1637+765_1637+766delinsCT	ENSP00000423877.2:n.1637+765_1637+766delinsCT
ENST00000697794.1:c.*1278+765_*1278+766delinsCT	ENSP00000513443.1:n.*1278+765_*1278+766delinsCT
ENST00000697799.1:n.1134+765_1134+766delinsCT
ENST00000698233.1:n.1366+765_1366+766delinsCT
ENST00000226574.9:c.1637+765_1637+766delinsCT MANE Select	ENSP00000226574.4:n.1637+765_1637+766delinsCT
ENST00000652569.1:c.1613+765_1613+766delinsCT
ENST00000652619.1:c.*164+765_*164+766delinsCT	ENSP00000499031.1:n.*164+765_*164+766delinsCT
ENST00000226574.8:c.1637+765_1637+766delinsCT	ENSP00000226574.4:n.1637+765_1637+766delinsCT
ENST00000394820.8:c.1634+765_1634+766delinsCT	ENSP00000378297.4:n.1634+765_1634+766delinsCT
ENST00000505458.5:c.1634+765_1634+766delinsCT	ENSP00000424790.1:n.1634+765_1634+766delinsCT
ENST00000600343.5:c.1094+765_1094+766delinsCT	ENSP00000469340.1:n.1094+765_1094+766delinsCT
NM_001165412.1:c.1634+765_1634+766delinsCT	NP_001158884.1:n.1634+765_1634+766delinsCT
NM_003998.3:c.1637+765_1637+766delinsCT	NP_003989.2:n.1637+765_1637+766delinsCT
XM_011532006.1:c.1658+765_1658+766delinsCT	XP_011530308.1:n.1658+765_1658+766delinsCT
XM_011532007.1:c.1634+765_1634+766delinsCT	XP_011530309.1:n.1634+765_1634+766delinsCT
XM_011532008.1:c.1478+765_1478+766delinsCT	XP_011530310.1:n.1478+765_1478+766delinsCT
XM_011532009.1:c.1241+765_1241+766delinsCT	XP_011530311.1:n.1241+765_1241+766delinsCT
XR_939027.1:n.3900_3901delinsAG
NM_001319226.1:c.1634+765_1634+766delinsCT	NP_001306155.1:n.1634+765_1634+766delinsCT
XM_011532006.2:c.1658+765_1658+766delinsCT	XP_011530308.1:n.1658+765_1658+766delinsCT
XM_024454067.1:c.1661+765_1661+766delinsCT	XP_024309835.1:n.1661+765_1661+766delinsCT
XM_024454068.1:c.1637+765_1637+766delinsCT	XP_024309836.1:n.1637+765_1637+766delinsCT
XM_024454069.1:c.1502+765_1502+766delinsCT	XP_024309837.1:n.1502+765_1502+766delinsCT
NM_003998.4:c.1637+765_1637+766delinsCT MANE Select	NP_003989.2:n.1637+765_1637+766delinsCT
NM_001165412.2:c.1634+765_1634+766delinsCT	NP_001158884.1:n.1634+765_1634+766delinsCT
NM_001319226.2:c.1634+765_1634+766delinsCT	NP_001306155.1:n.1634+765_1634+766delinsCT
NM_001382625.1:c.1637+765_1637+766delinsCT	NP_001369554.1:n.1637+765_1637+766delinsCT
NM_001382626.1:c.1637+765_1637+766delinsCT	NP_001369555.1:n.1637+765_1637+766delinsCT
NM_001382627.1:c.1634+765_1634+766delinsCT	NP_001369556.1:n.1634+765_1634+766delinsCT
NM_001382628.1:c.1595+765_1595+766delinsCT	NP_001369557.1:n.1595+765_1595+766delinsCT