Canonical Allele Identifier: CA2466733851

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561789G= , CM000685.2:g.154561789G=	GRCh38
NC_000023.10:g.153790004G= , CM000685.1:g.153790004G=	GRCh37
NC_000023.9:g.153443198G=	NCBI36
NG_009896.1:g.24546G= , LRG_70:g.24546G=

Transcript Alleles

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