Canonical Allele Identifier: CA2671578960

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102583074-GGCTTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102583076_102583081del , CM000666.2:g.102583076_102583081del	GRCh38
NC_000004.11:g.103504233_103504238del , CM000666.1:g.103504233_103504238del	GRCh37
NC_000004.10:g.103723271_103723276del	NCBI36
NG_050628.1:g.86748_86753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.951+119_951+124del	ENSP00000426147.2:n.951+119_951+124del
ENST00000509165.2:c.927+119_927+124del	ENSP00000423877.2:n.927+119_927+124del
ENST00000697794.1:c.*568+119_*568+124del	ENSP00000513443.1:n.*568+119_*568+124del
ENST00000697799.1:n.424+119_424+124del
ENST00000697800.1:n.138+119_138+124del
ENST00000226574.9:c.927+119_927+124del MANE Select	ENSP00000226574.4:n.927+119_927+124del
ENST00000652569.1:c.903+119_903+124del
ENST00000652619.1:c.948+119_948+124del	ENSP00000499031.1:n.948+119_948+124del
ENST00000226574.8:c.927+119_927+124del	ENSP00000226574.4:n.927+119_927+124del
ENST00000394820.8:c.924+119_924+124del	ENSP00000378297.4:n.924+119_924+124del
ENST00000505458.5:c.924+119_924+124del	ENSP00000424790.1:n.924+119_924+124del
ENST00000508584.1:c.306+119_306+124del	ENSP00000424815.1:n.306+119_306+124del
ENST00000600343.5:c.384+119_384+124del	ENSP00000469340.1:n.384+119_384+124del
NM_001165412.1:c.924+119_924+124del	NP_001158884.1:n.924+119_924+124del
NM_003998.3:c.927+119_927+124del	NP_003989.2:n.927+119_927+124del
XM_011532006.1:c.948+119_948+124del	XP_011530308.1:n.948+119_948+124del
XM_011532007.1:c.924+119_924+124del	XP_011530309.1:n.924+119_924+124del
XM_011532008.1:c.768+119_768+124del	XP_011530310.1:n.768+119_768+124del
XM_011532009.1:c.531+119_531+124del	XP_011530311.1:n.531+119_531+124del
NM_001319226.1:c.924+119_924+124del	NP_001306155.1:n.924+119_924+124del
XM_011532006.2:c.948+119_948+124del	XP_011530308.1:n.948+119_948+124del
XM_024454067.1:c.951+119_951+124del	XP_024309835.1:n.951+119_951+124del
XM_024454068.1:c.927+119_927+124del	XP_024309836.1:n.927+119_927+124del
XM_024454069.1:c.792+119_792+124del	XP_024309837.1:n.792+119_792+124del
NM_003998.4:c.927+119_927+124del MANE Select	NP_003989.2:n.927+119_927+124del
NM_001165412.2:c.924+119_924+124del	NP_001158884.1:n.924+119_924+124del
NM_001319226.2:c.924+119_924+124del	NP_001306155.1:n.924+119_924+124del
NM_001382625.1:c.927+119_927+124del	NP_001369554.1:n.927+119_927+124del
NM_001382626.1:c.927+119_927+124del	NP_001369555.1:n.927+119_927+124del
NM_001382627.1:c.924+119_924+124del	NP_001369556.1:n.924+119_924+124del
NM_001382628.1:c.885+119_885+124del	NP_001369557.1:n.885+119_885+124del