Canonical Allele Identifier: CA422814681

Gene: KIF21B

Linked Data

• MyVariant Identifiers: chr1:g.200960209T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991081T>A , CM000663.2:g.200991081T>A	GRCh38
NC_000001.10:g.200960209T>A , CM000663.1:g.200960209T>A	GRCh37
NC_000001.9:g.199226832T>A	NCBI36
NG_047130.1:g.37620A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461742.7:c.2523A>T MANE Select	ENSP00000433808.1:p.Pro841=
ENST00000332129.6:c.2523A>T	ENSP00000328494.2:p.Pro841=
ENST00000360529.9:c.2523A>T	ENSP00000353724.5:p.Pro841=
ENST00000422435.2:c.2523A>T	ENSP00000411831.2:p.Pro841=
ENST00000461742.6:c.2523A>T	ENSP00000433808.1:p.Pro841=
NM_001252100.1:c.2523A>T	NP_001239029.1:p.Pro841=
NM_001252102.1:c.2523A>T	NP_001239031.1:p.Pro841=
NM_001252103.1:c.2523A>T	NP_001239032.1:p.Pro841=
NM_017596.3:c.2523A>T	NP_060066.2:p.Pro841=
XR_921754.1:n.2629A>T
XR_921755.1:n.2462A>T
XR_921756.1:n.1597A>T
XR_921757.1:n.1624A>T
XR_921758.1:n.956A>T
XM_017000731.1:c.2355A>T	XP_016856220.1:p.Pro785=
XM_017000732.1:c.1320A>T	XP_016856221.1:p.Pro440=
NM_001252100.2:c.2523A>T	NP_001239029.1:p.Pro841=
NM_001252102.2:c.2523A>T MANE Select	NP_001239031.1:p.Pro841=
NM_001252103.2:c.2523A>T	NP_001239032.1:p.Pro841=
NM_017596.4:c.2523A>T	NP_060066.2:p.Pro841=