Canonical Allele Identifier: CA2483008286
Gene: IKBKE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206484465T>A , CM000663.2:g.206484465T>A GRCh38
NC_000001.10:g.206657802T>A , CM000663.1:g.206657802T>A GRCh37
NC_000001.9:g.204724425T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000581977.7:c.1428-532T>A MANE Select ENSP00000464030.1:n.1428-532T>A
ENST00000578328.6:c.1428-532T>A ENSP00000473833.1:n.1428-532T>A
ENST00000581977.6:c.1428-532T>A ENSP00000464030.1:n.1428-532T>A
ENST00000584998.5:c.1173-532T>A ENSP00000462396.1:n.1173-532T>A
NM_001193321.1:c.1173-532T>A NP_001180250.1:n.1173-532T>A
NM_001193322.1:c.1428-532T>A NP_001180251.1:n.1428-532T>A
NM_014002.3:c.1428-532T>A NP_054721.1:n.1428-532T>A
XM_005273356.2:c.1428-532T>A XP_005273413.1:n.1428-532T>A
XR_922002.1:n.1802-532T>A
XM_017002868.1:c.1062-532T>A XP_016858357.1:n.1062-532T>A
XR_922002.2:n.1780-532T>A
NM_014002.4:c.1428-532T>A MANE Select NP_054721.1:n.1428-532T>A
NM_001193321.2:c.1173-532T>A NP_001180250.1:n.1173-532T>A
NM_001193322.2:c.1428-532T>A NP_001180251.1:n.1428-532T>A