Canonical Allele Identifier: CA2171863705
Gene: KNL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40621836_40621839delinsGACC , CM000677.2:g.40621836_40621839delinsGACC GRCh38
NC_000015.9:g.40914034_40914037delinsGACC , CM000677.1:g.40914034_40914037delinsGACC GRCh37
NC_000015.8:g.38701326_38701329delinsGACC NCBI36
NG_033114.1:g.32588_32591delinsGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.1572_1575delinsGACC MANE Select ENSP00000382576.3:p.Met524=
ENST00000346991.9:c.1650_1653delinsGACC ENSP00000335463.6:p.Met550=
ENST00000399668.6:c.1572_1575delinsGACC ENSP00000382576.2:p.Met524=
ENST00000527044.5:c.1572_1575delinsGACC ENSP00000432654.2:p.Met524=
ENST00000533001.1:n.1717_1720delinsGACC
ENST00000534204.1:c.116-7488_116-7485delinsGACC ENSP00000453857.1:n.116-7488_116-7485delinsGACC
ENST00000614337.4:n.1888_1891delinsGACC
NM_144508.4:c.1572_1575delinsGACC NP_653091.3:p.Met524=
NM_170589.4:c.1650_1653delinsGACC NP_733468.3:p.Met550=
XM_011521816.1:c.1248_1251delinsGACC XP_011520118.1:p.Met416=
XM_011521817.1:c.1572_1575delinsGACC XP_011520119.1:p.Met524=
XM_017022432.1:c.1248_1251delinsGACC XP_016877921.1:p.Met416=
NM_144508.5:c.1572_1575delinsGACC MANE Select NP_653091.3:p.Met524=
NM_170589.5:c.1650_1653delinsGACC NP_733468.3:p.Met550=