Canonical Allele Identifier: CA1320950
Gene: KIF21B HGNC NCBI

Linked Data

dbSNP Id: rs141349980

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200991089G>A , CM000663.2:g.200991089G>A GRCh38
NC_000001.10:g.200960217G>A , CM000663.1:g.200960217G>A GRCh37
NC_000001.9:g.199226840G>A NCBI36
NG_047130.1:g.37612C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461742.7:c.2515C>T MANE Select ENSP00000433808.1:p.Leu839=
ENST00000332129.6:c.2515C>T ENSP00000328494.2:p.Leu839=
ENST00000360529.9:c.2515C>T ENSP00000353724.5:p.Leu839=
ENST00000422435.2:c.2515C>T ENSP00000411831.2:p.Leu839=
ENST00000461742.6:c.2515C>T ENSP00000433808.1:p.Leu839=
NM_001252100.1:c.2515C>T NP_001239029.1:p.Leu839=
NM_001252102.1:c.2515C>T NP_001239031.1:p.Leu839=
NM_001252103.1:c.2515C>T NP_001239032.1:p.Leu839=
NM_017596.3:c.2515C>T NP_060066.2:p.Leu839=
XR_921754.1:n.2621C>T
XR_921755.1:n.2454C>T
XR_921756.1:n.1589C>T
XR_921757.1:n.1616C>T
XR_921758.1:n.948C>T
XM_017000731.1:c.2347C>T XP_016856220.1:p.Leu783=
XM_017000732.1:c.1312C>T XP_016856221.1:p.Leu438=
NM_001252100.2:c.2515C>T NP_001239029.1:p.Leu839=
NM_001252102.2:c.2515C>T MANE Select NP_001239031.1:p.Leu839=
NM_001252103.2:c.2515C>T NP_001239032.1:p.Leu839=
NM_017596.4:c.2515C>T NP_060066.2:p.Leu839=