Canonical Allele Identifier: CA344138565
Gene: KIF21B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200991082G>C , CM000663.2:g.200991082G>C GRCh38
NC_000001.10:g.200960210G>C , CM000663.1:g.200960210G>C GRCh37
NC_000001.9:g.199226833G>C NCBI36
NG_047130.1:g.37619C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461742.7:c.2522C>G MANE Select ENSP00000433808.1:p.Pro841Arg
ENST00000332129.6:c.2522C>G ENSP00000328494.2:p.Pro841Arg
ENST00000360529.9:c.2522C>G ENSP00000353724.5:p.Pro841Arg
ENST00000422435.2:c.2522C>G ENSP00000411831.2:p.Pro841Arg
ENST00000461742.6:c.2522C>G ENSP00000433808.1:p.Pro841Arg
NM_001252100.1:c.2522C>G NP_001239029.1:p.Pro841Arg
NM_001252102.1:c.2522C>G NP_001239031.1:p.Pro841Arg
NM_001252103.1:c.2522C>G NP_001239032.1:p.Pro841Arg
NM_017596.3:c.2522C>G NP_060066.2:p.Pro841Arg
XR_921754.1:n.2628C>G
XR_921755.1:n.2461C>G
XR_921756.1:n.1596C>G
XR_921757.1:n.1623C>G
XR_921758.1:n.955C>G
XM_017000731.1:c.2354C>G XP_016856220.1:p.Pro785Arg
XM_017000732.1:c.1319C>G XP_016856221.1:p.Pro440Arg
NM_001252100.2:c.2522C>G NP_001239029.1:p.Pro841Arg
NM_001252102.2:c.2522C>G MANE Select NP_001239031.1:p.Pro841Arg
NM_001252103.2:c.2522C>G NP_001239032.1:p.Pro841Arg
NM_017596.4:c.2522C>G NP_060066.2:p.Pro841Arg