Canonical Allele Identifier: CA344138550

Gene: KIF21B

Linked Data

• ClinVar Variation Id: 2293344
• ClinVar RCV Id: RCV004142450
• MyVariant Identifiers: chr1:g.200960207G>C (hg19) ; chr1:g.200991079G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991079G>C , CM000663.2:g.200991079G>C	GRCh38
NC_000001.10:g.200960207G>C , CM000663.1:g.200960207G>C	GRCh37
NC_000001.9:g.199226830G>C	NCBI36
NG_047130.1:g.37622C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461742.7:c.2525C>G MANE Select	ENSP00000433808.1:p.Pro842Arg
ENST00000332129.6:c.2525C>G	ENSP00000328494.2:p.Pro842Arg
ENST00000360529.9:c.2525C>G	ENSP00000353724.5:p.Pro842Arg
ENST00000422435.2:c.2525C>G	ENSP00000411831.2:p.Pro842Arg
ENST00000461742.6:c.2525C>G	ENSP00000433808.1:p.Pro842Arg
NM_001252100.1:c.2525C>G	NP_001239029.1:p.Pro842Arg
NM_001252102.1:c.2525C>G	NP_001239031.1:p.Pro842Arg
NM_001252103.1:c.2525C>G	NP_001239032.1:p.Pro842Arg
NM_017596.3:c.2525C>G	NP_060066.2:p.Pro842Arg
XR_921754.1:n.2631C>G
XR_921755.1:n.2464C>G
XR_921756.1:n.1599C>G
XR_921757.1:n.1626C>G
XR_921758.1:n.958C>G
XM_017000731.1:c.2357C>G	XP_016856220.1:p.Pro786Arg
XM_017000732.1:c.1322C>G	XP_016856221.1:p.Pro441Arg
NM_001252100.2:c.2525C>G	NP_001239029.1:p.Pro842Arg
NM_001252102.2:c.2525C>G MANE Select	NP_001239031.1:p.Pro842Arg
NM_001252103.2:c.2525C>G	NP_001239032.1:p.Pro842Arg
NM_017596.4:c.2525C>G	NP_060066.2:p.Pro842Arg