Canonical Allele Identifier: CA2483003921
Gene: IKBKE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206474107A>T , CM000663.2:g.206474107A>T GRCh38
NC_000001.10:g.206647450A>T , CM000663.1:g.206647450A>T GRCh37
NC_000001.9:g.204714073A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000581977.7:c.88-224A>T MANE Select ENSP00000464030.1:n.88-224A>T
ENST00000578328.6:c.88-224A>T ENSP00000473833.1:n.88-224A>T
ENST00000579827.6:c.88-224A>T ENSP00000474422.1:n.88-224A>T
ENST00000581977.6:c.88-224A>T ENSP00000464030.1:n.88-224A>T
ENST00000584998.5:c.-168-224A>T ENSP00000462396.1:n.-168-224A>T
ENST00000605726.1:c.88-224A>T ENSP00000474229.1:n.88-224A>T
ENST00000605818.5:n.433-224A>T
NM_001193321.1:c.-168-224A>T NP_001180250.1:n.-168-224A>T
NM_001193322.1:c.88-224A>T NP_001180251.1:n.88-224A>T
NM_014002.3:c.88-224A>T NP_054721.1:n.88-224A>T
XM_005273356.2:c.88-224A>T XP_005273413.1:n.88-224A>T
XR_922002.1:n.462-224A>T
XM_017002868.1:c.-394-224A>T XP_016858357.1:n.-394-224A>T
XR_922002.2:n.440-224A>T
NM_014002.4:c.88-224A>T MANE Select NP_054721.1:n.88-224A>T
NM_001193321.2:c.-168-224A>T NP_001180250.1:n.-168-224A>T
NM_001193322.2:c.88-224A>T NP_001180251.1:n.88-224A>T