Canonical Allele Identifier: CA129111
Gene: KIF22 HGNC NCBI

Linked Data

ClinVar Variation Id: 30333
dbSNP Id: rs193922920

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.29798640C>T , CM000678.2:g.29798640C>T GRCh38
NC_000016.9:g.29809961C>T , CM000678.1:g.29809961C>T GRCh37
NC_000016.8:g.29717462C>T NCBI36
NG_032055.1:g.12928C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000561482.6:c.238C>T ENSP00000454957.1:p.Pro80Ser
ENST00000563263.2:n.827C>T
ENST00000563666.2:n.471C>T
ENST00000569382.3:c.442C>T ENSP00000456165.3:p.Pro148Ser
ENST00000569636.7:c.437C>T ENSP00000457176.3:p.Pro146Leu
ENST00000570173.6:c.*177C>T ENSP00000455702.1:n.*177C>T
ENST00000685401.1:c.442C>T ENSP00000509077.1:p.Pro148Ser
ENST00000685526.1:c.442C>T ENSP00000510465.1:p.Pro148Ser
ENST00000685961.1:c.176C>T
ENST00000686384.1:n.454C>T
ENST00000687634.1:c.176C>T
ENST00000688492.1:n.319C>T
ENST00000689089.1:c.442C>T ENSP00000509109.1:p.Pro148Ser
ENST00000689107.1:c.442C>T ENSP00000509175.1:p.Pro148Ser
ENST00000689172.1:c.442C>T ENSP00000508827.1:p.Pro148Ser
ENST00000689660.1:c.442C>T ENSP00000509285.1:p.Pro148Ser
ENST00000689743.1:n.471C>T
ENST00000690258.1:c.238C>T ENSP00000509977.1:p.Pro80Ser
ENST00000690419.1:c.442C>T ENSP00000509446.1:p.Pro148Ser
ENST00000690510.1:n.451C>T
ENST00000691128.1:c.442C>T ENSP00000509922.1:p.Pro148Ser
ENST00000691169.1:n.475C>T
ENST00000691203.1:n.452C>T
ENST00000691486.1:c.176C>T
ENST00000691895.1:c.442C>T ENSP00000510045.1:p.Pro148Ser
ENST00000693260.1:c.442C>T ENSP00000509562.1:p.Pro148Ser
ENST00000160827.9:c.442C>T MANE Select ENSP00000160827.5:p.Pro148Ser
ENST00000160827.8:c.442C>T ENSP00000160827.4:p.Pro148Ser
ENST00000400751.9:c.238C>T ENSP00000383562.5:p.Pro80Ser
ENST00000561482.5:c.238C>T ENSP00000454957.1:p.Pro80Ser
ENST00000563666.1:n.277C>T
ENST00000569382.2:c.238C>T ENSP00000456165.2:p.Pro80Ser
ENST00000569636.6:c.238C>T ENSP00000457176.2:p.Pro80Ser
ENST00000570173.5:c.*177C>T ENSP00000455702.1:n.*177C>T
NM_001256269.1:c.238C>T NP_001243198.1:p.Pro80Ser
NM_001256270.1:c.238C>T NP_001243199.1:p.Pro80Ser
NM_007317.2:c.442C>T NP_015556.1:p.Pro148Ser
XR_243280.2:n.1140C>T
XM_024450270.1:c.442C>T XP_024306038.1:p.Pro148Ser
XR_243280.4:n.468C>T
NM_001256269.2:c.238C>T NP_001243198.1:p.Pro80Ser
NM_007317.3:c.442C>T MANE Select NP_015556.1:p.Pro148Ser