Canonical Allele Identifier: CA1140366564

Gene: KIF21B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201015352G= , CM000663.2:g.201015352G=	GRCh38
NC_000001.10:g.200984480G= , CM000663.1:g.200984480G=	GRCh37
NC_000001.9:g.199251103G=	NCBI36
NG_047130.1:g.13349C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001252102.2:c.42-5864C= MANE Select	NP_001239031.1:n.42-5864C=
ENST00000461742.7:c.42-5864C= MANE Select	ENSP00000433808.1:n.42-5864C=
NM_001252100.1:c.42-5864C=	NP_001239029.1:n.42-5864C=
NM_001252100.2:c.42-5864C=	NP_001239029.1:n.42-5864C=
NM_001252102.1:c.42-5864C=	NP_001239031.1:n.42-5864C=
NM_001252103.1:c.42-5864C=	NP_001239032.1:n.42-5864C=
NM_001252103.2:c.42-5864C=	NP_001239032.1:n.42-5864C=
NM_017596.3:c.42-5864C=	NP_060066.2:n.42-5864C=
NM_017596.4:c.42-5864C=	NP_060066.2:n.42-5864C=
ENST00000332129.6:c.42-5864C=	ENSP00000328494.2:n.42-5864C=
ENST00000360529.9:c.42-5864C=	ENSP00000353724.5:n.42-5864C=
ENST00000422435.2:c.42-5864C=	ENSP00000411831.2:n.42-5864C=
ENST00000461742.6:c.42-5864C=	ENSP00000433808.1:n.42-5864C=
XM_017000731.1:c.42-5864C=	XP_016856220.1:n.42-5864C=
XR_921754.1:n.148-5864C=
XR_921755.1:n.149-5864C=