Canonical Allele Identifier: CA1219539538
Gene: KIF21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200991183A= , CM000663.2:g.200991183A= GRCh38
NC_000001.10:g.200960311A= , CM000663.1:g.200960311A= GRCh37
NC_000001.9:g.199226934A= NCBI36
NG_047130.1:g.37518T=

Transcript Alleles

HGVS Amino-acid change
ENST00000461742.7:c.2455-34T= MANE Select ENSP00000433808.1:n.2455-34T=
ENST00000332129.6:c.2455-34T= ENSP00000328494.2:n.2455-34T=
ENST00000360529.9:c.2455-34T= ENSP00000353724.5:n.2455-34T=
ENST00000422435.2:c.2455-34T= ENSP00000411831.2:n.2455-34T=
ENST00000461742.6:c.2455-34T= ENSP00000433808.1:n.2455-34T=
NM_001252100.1:c.2455-34T= NP_001239029.1:n.2455-34T=
NM_001252102.1:c.2455-34T= NP_001239031.1:n.2455-34T=
NM_001252103.1:c.2455-34T= NP_001239032.1:n.2455-34T=
NM_017596.3:c.2455-34T= NP_060066.2:n.2455-34T=
XR_921754.1:n.2561-34T=
XR_921755.1:n.2394-34T=
XR_921756.1:n.1529-34T=
XR_921757.1:n.1556-34T=
XR_921758.1:n.888-34T=
XM_017000731.1:c.2287-34T= XP_016856220.1:n.2287-34T=
XM_017000732.1:c.1252-34T= XP_016856221.1:n.1252-34T=
NM_001252100.2:c.2455-34T= NP_001239029.1:n.2455-34T=
NM_001252102.2:c.2455-34T= MANE Select NP_001239031.1:n.2455-34T=
NM_001252103.2:c.2455-34T= NP_001239032.1:n.2455-34T=
NM_017596.4:c.2455-34T= NP_060066.2:n.2455-34T=