Canonical Allele Identifier: CA489773011
Gene: KNL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40943732A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651534A>G , CM000677.2:g.40651534A>G GRCh38
NC_000015.9:g.40943732A>G , CM000677.1:g.40943732A>G GRCh37
NC_000015.8:g.38731024A>G NCBI36
NG_033114.1:g.62286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6276A>G MANE Select ENSP00000382576.3:p.Lys2092=
ENST00000346991.9:c.6354A>G ENSP00000335463.6:p.Lys2118=
ENST00000399668.6:c.6276A>G ENSP00000382576.2:p.Lys2092=
ENST00000526913.5:c.3409A>G
ENST00000532347.1:n.356A>G
NM_144508.4:c.6276A>G NP_653091.3:p.Lys2092=
NM_170589.4:c.6354A>G NP_733468.3:p.Lys2118=
XM_011521816.1:c.5952A>G XP_011520118.1:p.Lys1984=
XM_011521817.1:c.6276A>G XP_011520119.1:p.Lys2092=
XM_017022432.1:c.5952A>G XP_016877921.1:p.Lys1984=
NM_144508.5:c.6276A>G MANE Select NP_653091.3:p.Lys2092=
NM_170589.5:c.6354A>G NP_733468.3:p.Lys2118=