Canonical Allele Identifier: CA344138558

Gene: KIF21B

Linked Data

• MyVariant Identifiers: chr1:g.200960208G>T (hg19) ; chr1:g.200991080G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991080G>T , CM000663.2:g.200991080G>T	GRCh38
NC_000001.10:g.200960208G>T , CM000663.1:g.200960208G>T	GRCh37
NC_000001.9:g.199226831G>T	NCBI36
NG_047130.1:g.37621C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461742.7:c.2524C>A MANE Select	ENSP00000433808.1:p.Pro842Thr
ENST00000332129.6:c.2524C>A	ENSP00000328494.2:p.Pro842Thr
ENST00000360529.9:c.2524C>A	ENSP00000353724.5:p.Pro842Thr
ENST00000422435.2:c.2524C>A	ENSP00000411831.2:p.Pro842Thr
ENST00000461742.6:c.2524C>A	ENSP00000433808.1:p.Pro842Thr
NM_001252100.1:c.2524C>A	NP_001239029.1:p.Pro842Thr
NM_001252102.1:c.2524C>A	NP_001239031.1:p.Pro842Thr
NM_001252103.1:c.2524C>A	NP_001239032.1:p.Pro842Thr
NM_017596.3:c.2524C>A	NP_060066.2:p.Pro842Thr
XR_921754.1:n.2630C>A
XR_921755.1:n.2463C>A
XR_921756.1:n.1598C>A
XR_921757.1:n.1625C>A
XR_921758.1:n.957C>A
XM_017000731.1:c.2356C>A	XP_016856220.1:p.Pro786Thr
XM_017000732.1:c.1321C>A	XP_016856221.1:p.Pro441Thr
NM_001252100.2:c.2524C>A	NP_001239029.1:p.Pro842Thr
NM_001252102.2:c.2524C>A MANE Select	NP_001239031.1:p.Pro842Thr
NM_001252103.2:c.2524C>A	NP_001239032.1:p.Pro842Thr
NM_017596.4:c.2524C>A	NP_060066.2:p.Pro842Thr