Canonical Allele Identifier: CA422814687

Gene: KIF21B

Linked Data

• gnomAD v4: 1-200991090-T-A
• MyVariant Identifiers: chr1:g.200960218T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991090T>A , CM000663.2:g.200991090T>A	GRCh38
NC_000001.10:g.200960218T>A , CM000663.1:g.200960218T>A	GRCh37
NC_000001.9:g.199226841T>A	NCBI36
NG_047130.1:g.37611A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461742.7:c.2514A>T MANE Select	ENSP00000433808.1:p.Gly838=
ENST00000332129.6:c.2514A>T	ENSP00000328494.2:p.Gly838=
ENST00000360529.9:c.2514A>T	ENSP00000353724.5:p.Gly838=
ENST00000422435.2:c.2514A>T	ENSP00000411831.2:p.Gly838=
ENST00000461742.6:c.2514A>T	ENSP00000433808.1:p.Gly838=
NM_001252100.1:c.2514A>T	NP_001239029.1:p.Gly838=
NM_001252102.1:c.2514A>T	NP_001239031.1:p.Gly838=
NM_001252103.1:c.2514A>T	NP_001239032.1:p.Gly838=
NM_017596.3:c.2514A>T	NP_060066.2:p.Gly838=
XR_921754.1:n.2620A>T
XR_921755.1:n.2453A>T
XR_921756.1:n.1588A>T
XR_921757.1:n.1615A>T
XR_921758.1:n.947A>T
XM_017000731.1:c.2346A>T	XP_016856220.1:p.Gly782=
XM_017000732.1:c.1311A>T	XP_016856221.1:p.Gly437=
NM_001252100.2:c.2514A>T	NP_001239029.1:p.Gly838=
NM_001252102.2:c.2514A>T MANE Select	NP_001239031.1:p.Gly838=
NM_001252103.2:c.2514A>T	NP_001239032.1:p.Gly838=
NM_017596.4:c.2514A>T	NP_060066.2:p.Gly838=