Canonical Allele Identifier: CA344117443

Gene: KIF21B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201008783C>G , CM000663.2:g.201008783C>G	GRCh38
NC_000001.10:g.200977911C>G , CM000663.1:g.200977911C>G	GRCh37
NC_000001.9:g.199244534C>G	NCBI36
NG_047130.1:g.19918G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001252102.2:c.433G>C MANE Select	NP_001239031.1:p.Ala145Pro
ENST00000461742.7:c.433G>C MANE Select	ENSP00000433808.1:p.Ala145Pro
NM_001252100.1:c.433G>C	NP_001239029.1:p.Ala145Pro
NM_001252100.2:c.433G>C	NP_001239029.1:p.Ala145Pro
NM_001252102.1:c.433G>C	NP_001239031.1:p.Ala145Pro
NM_001252103.1:c.433G>C	NP_001239032.1:p.Ala145Pro
NM_001252103.2:c.433G>C	NP_001239032.1:p.Ala145Pro
NM_017596.3:c.433G>C	NP_060066.2:p.Ala145Pro
NM_017596.4:c.433G>C	NP_060066.2:p.Ala145Pro
ENST00000332129.6:c.433G>C	ENSP00000328494.2:p.Ala145Pro
ENST00000360529.9:c.433G>C	ENSP00000353724.5:p.Ala145Pro
ENST00000422435.2:c.433G>C	ENSP00000411831.2:p.Ala145Pro
ENST00000461742.6:c.433G>C	ENSP00000433808.1:p.Ala145Pro
XM_017000731.1:c.433G>C	XP_016856220.1:p.Ala145Pro
XR_921754.1:n.539G>C
XR_921755.1:n.540G>C