Canonical Allele Identifier: CA2216284813

Gene: KIF22

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29798644G= , CM000678.2:g.29798644G=	GRCh38
NC_000016.9:g.29809965G= , CM000678.1:g.29809965G=	GRCh37
NC_000016.8:g.29717466G=	NCBI36
NG_032055.1:g.12932G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561482.6:c.242G=	ENSP00000454957.1:p.Arg81=
ENST00000563263.2:n.831G=
ENST00000563666.2:n.475G=
ENST00000569382.3:c.446G=	ENSP00000456165.3:p.Arg149=
ENST00000569636.7:c.441G=	ENSP00000457176.3:p.Ala147=
ENST00000570173.6:c.*181G=	ENSP00000455702.1:n.*181G=
ENST00000685401.1:c.446G=	ENSP00000509077.1:p.Arg149=
ENST00000685526.1:c.446G=	ENSP00000510465.1:p.Arg149=
ENST00000685961.1:c.180G=
ENST00000686384.1:n.458G=
ENST00000687634.1:c.180G=
ENST00000688492.1:n.323G=
ENST00000689089.1:c.446G=	ENSP00000509109.1:p.Arg149=
ENST00000689107.1:c.446G=	ENSP00000509175.1:p.Arg149=
ENST00000689172.1:c.446G=	ENSP00000508827.1:p.Arg149=
ENST00000689660.1:c.446G=	ENSP00000509285.1:p.Arg149=
ENST00000689743.1:n.475G=
ENST00000690258.1:c.242G=	ENSP00000509977.1:p.Arg81=
ENST00000690419.1:c.446G=	ENSP00000509446.1:p.Arg149=
ENST00000690510.1:n.455G=
ENST00000691128.1:c.446G=	ENSP00000509922.1:p.Arg149=
ENST00000691169.1:n.479G=
ENST00000691203.1:n.456G=
ENST00000691486.1:c.180G=
ENST00000691895.1:c.446G=	ENSP00000510045.1:p.Arg149=
ENST00000693260.1:c.446G=	ENSP00000509562.1:p.Arg149=
ENST00000160827.9:c.446G= MANE Select	ENSP00000160827.5:p.Arg149=
ENST00000160827.8:c.446G=	ENSP00000160827.4:p.Arg149=
ENST00000400751.9:c.242G=	ENSP00000383562.5:p.Arg81=
ENST00000561482.5:c.242G=	ENSP00000454957.1:p.Arg81=
ENST00000563666.1:n.281G=
ENST00000569382.2:c.242G=	ENSP00000456165.2:p.Arg81=
ENST00000569636.6:c.242G=	ENSP00000457176.2:p.Arg81=
ENST00000570173.5:c.*181G=	ENSP00000455702.1:n.*181G=
NM_001256269.1:c.242G=	NP_001243198.1:p.Arg81=
NM_001256270.1:c.242G=	NP_001243199.1:p.Arg81=
NM_007317.2:c.446G=	NP_015556.1:p.Arg149=
XR_243280.2:n.1144G=
XM_024450270.1:c.446G=	XP_024306038.1:p.Arg149=
XR_243280.4:n.472G=
NM_001256269.2:c.242G=	NP_001243198.1:p.Arg81=
NM_007317.3:c.446G= MANE Select	NP_015556.1:p.Arg149=