Canonical Allele Identifier: CA344138570

Gene: KIF21B

Linked Data

• MyVariant Identifiers: chr1:g.200960211G>A (hg19) ; chr1:g.200991083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991083G>A , CM000663.2:g.200991083G>A	GRCh38
NC_000001.10:g.200960211G>A , CM000663.1:g.200960211G>A	GRCh37
NC_000001.9:g.199226834G>A	NCBI36
NG_047130.1:g.37618C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461742.7:c.2521C>T MANE Select	ENSP00000433808.1:p.Pro841Ser
ENST00000332129.6:c.2521C>T	ENSP00000328494.2:p.Pro841Ser
ENST00000360529.9:c.2521C>T	ENSP00000353724.5:p.Pro841Ser
ENST00000422435.2:c.2521C>T	ENSP00000411831.2:p.Pro841Ser
ENST00000461742.6:c.2521C>T	ENSP00000433808.1:p.Pro841Ser
NM_001252100.1:c.2521C>T	NP_001239029.1:p.Pro841Ser
NM_001252102.1:c.2521C>T	NP_001239031.1:p.Pro841Ser
NM_001252103.1:c.2521C>T	NP_001239032.1:p.Pro841Ser
NM_017596.3:c.2521C>T	NP_060066.2:p.Pro841Ser
XR_921754.1:n.2627C>T
XR_921755.1:n.2460C>T
XR_921756.1:n.1595C>T
XR_921757.1:n.1622C>T
XR_921758.1:n.954C>T
XM_017000731.1:c.2353C>T	XP_016856220.1:p.Pro785Ser
XM_017000732.1:c.1318C>T	XP_016856221.1:p.Pro440Ser
NM_001252100.2:c.2521C>T	NP_001239029.1:p.Pro841Ser
NM_001252102.2:c.2521C>T MANE Select	NP_001239031.1:p.Pro841Ser
NM_001252103.2:c.2521C>T	NP_001239032.1:p.Pro841Ser
NM_017596.4:c.2521C>T	NP_060066.2:p.Pro841Ser