Canonical Allele Identifier: CA2695237083

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561789_154561794del , CM000685.2:g.154561789_154561794del	GRCh38
NC_000023.10:g.153790004_153790009del , CM000685.1:g.153790004_153790009del	GRCh37
NC_000023.9:g.153443198_153443203del	NCBI36
NG_009896.1:g.24546_24551del , LRG_70:g.24546_24551del

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.732+5_732+10del	ENSP00000398579.2:n.732+5_732+10del
ENST00000422680.6:c.768+5_768+10del	ENSP00000390368.3:n.768+5_768+10del
ENST00000440286.6:c.768+5_768+10del	ENSP00000394934.2:n.768+5_768+10del
ENST00000445622.6:c.768+5_768+10del	ENSP00000395205.2:n.768+5_768+10del
ENST00000615186.5:c.366+5_366+10del	ENSP00000479144.2:n.366+5_366+10del
ENST00000686774.1:c.*149+5_*149+10del	ENSP00000510218.1:n.*149+5_*149+10del
ENST00000687445.1:n.1145_1150del
ENST00000689906.1:c.615+5_615+10del	ENSP00000508630.1:n.615+5_615+10del
ENST00000692948.1:c.825+5_825+10del	ENSP00000508773.1:n.825+5_825+10del
ENST00000693029.1:n.1148_1153del
ENST00000594239.6:c.768+5_768+10del MANE Select	ENSP00000471166.1:n.768+5_768+10del
ENST00000594239.5:c.768+5_768+10del	ENSP00000471166.1:n.768+5_768+10del
ENST00000611071.4:c.768+5_768+10del	ENSP00000479662.1:n.768+5_768+10del
ENST00000611176.4:c.615+5_615+10del	ENSP00000478616.1:n.615+5_615+10del
ENST00000612051.1:c.*760+5_*760+10del	ENSP00000480431.1:n.*760+5_*760+10del
ENST00000615874.4:c.744+26_744+31del	ENSP00000483381.1:n.744+26_744+31del
ENST00000617207.4:c.765+5_765+10del	ENSP00000484023.1:n.765+5_765+10del
ENST00000617838.1:n.200-1021_200-1016del
ENST00000618670.4:c.972+5_972+10del	ENSP00000483825.1:n.972+5_972+10del
ENST00000619941.4:c.747+26_747+31del	ENSP00000478979.1:n.747+26_747+31del
NM_001099856.3:c.972+5_972+10del	NP_001093326.2:n.972+5_972+10del
NM_001099857.2:c.768+5_768+10del	NP_001093327.1:n.768+5_768+10del
NM_001145255.2:c.615+5_615+10del	NP_001138727.1:n.615+5_615+10del
NM_003639.4:c.768+5_768+10del	NP_003630.1:n.768+5_768+10del
XM_005274760.3:c.969+5_969+10del	XP_005274817.1:n.969+5_969+10del
XM_005274761.3:c.972+5_972+10del	XP_005274818.1:n.972+5_972+10del
XM_005274764.3:c.765+5_765+10del	XP_005274821.1:n.765+5_765+10del
XM_011531203.1:c.819+5_819+10del	XP_011529505.1:n.819+5_819+10del
XM_011531204.1:c.768+5_768+10del	XP_011529506.1:n.768+5_768+10del
XM_011531205.1:c.768+5_768+10del	XP_011529507.1:n.768+5_768+10del
NM_001099856.4:c.972+5_972+10del	NP_001093326.2:n.972+5_972+10del
NM_001321396.1:c.768+5_768+10del	NP_001308325.1:n.768+5_768+10del
NM_001321397.1:c.765+5_765+10del	NP_001308326.1:n.765+5_765+10del
NM_001099856.6:c.972+5_972+10del	NP_001093326.2:n.972+5_972+10del
NM_001099857.4:c.768+5_768+10del	NP_001093327.1:n.768+5_768+10del
NM_001145255.4:c.615+5_615+10del	NP_001138727.1:n.615+5_615+10del
NM_001321396.3:c.768+5_768+10del	NP_001308325.1:n.768+5_768+10del
NM_001321397.3:c.765+5_765+10del	NP_001308326.1:n.765+5_765+10del
NM_001377312.1:c.768+5_768+10del	NP_001364241.1:n.768+5_768+10del
NM_001377313.1:c.765+5_765+10del	NP_001364242.1:n.765+5_765+10del
NM_001377314.1:c.612+5_612+10del	NP_001364243.1:n.612+5_612+10del
NM_001377315.1:c.400-1021_400-1016del	NP_001364244.1:n.400-1021_400-1016del
NR_165197.1:n.637+5_637+10del
NM_001099857.5:c.768+5_768+10del MANE Select	NP_001093327.1:n.768+5_768+10del