Canonical Allele Identifier: CA422814683

Gene: KIF21B

Linked Data

• gnomAD v4: 1-200991087-T-G
• MyVariant Identifiers: chr1:g.200960215T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200991087T>G , CM000663.2:g.200991087T>G	GRCh38
NC_000001.10:g.200960215T>G , CM000663.1:g.200960215T>G	GRCh37
NC_000001.9:g.199226838T>G	NCBI36
NG_047130.1:g.37614A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461742.7:c.2517A>C MANE Select	ENSP00000433808.1:p.Leu839=
ENST00000332129.6:c.2517A>C	ENSP00000328494.2:p.Leu839=
ENST00000360529.9:c.2517A>C	ENSP00000353724.5:p.Leu839=
ENST00000422435.2:c.2517A>C	ENSP00000411831.2:p.Leu839=
ENST00000461742.6:c.2517A>C	ENSP00000433808.1:p.Leu839=
NM_001252100.1:c.2517A>C	NP_001239029.1:p.Leu839=
NM_001252102.1:c.2517A>C	NP_001239031.1:p.Leu839=
NM_001252103.1:c.2517A>C	NP_001239032.1:p.Leu839=
NM_017596.3:c.2517A>C	NP_060066.2:p.Leu839=
XR_921754.1:n.2623A>C
XR_921755.1:n.2456A>C
XR_921756.1:n.1591A>C
XR_921757.1:n.1618A>C
XR_921758.1:n.950A>C
XM_017000731.1:c.2349A>C	XP_016856220.1:p.Leu783=
XM_017000732.1:c.1314A>C	XP_016856221.1:p.Leu438=
NM_001252100.2:c.2517A>C	NP_001239029.1:p.Leu839=
NM_001252102.2:c.2517A>C MANE Select	NP_001239031.1:p.Leu839=
NM_001252103.2:c.2517A>C	NP_001239032.1:p.Leu839=
NM_017596.4:c.2517A>C	NP_060066.2:p.Leu839=