Canonical Allele Identifier: CA391732273
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40621787T>C , CM000677.2:g.40621787T>C GRCh38
NC_000015.9:g.40913985T>C , CM000677.1:g.40913985T>C GRCh37
NC_000015.8:g.38701277T>C NCBI36
NG_033114.1:g.32539T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.1523T>C MANE Select ENSP00000382576.3:p.Ile508Thr
ENST00000346991.9:c.1601T>C ENSP00000335463.6:p.Ile534Thr
ENST00000399668.6:c.1523T>C ENSP00000382576.2:p.Ile508Thr
ENST00000527044.5:c.1523T>C ENSP00000432654.2:p.Ile508Thr
ENST00000533001.1:n.1668T>C
ENST00000534204.1:c.116-7537T>C ENSP00000453857.1:n.116-7537T>C
ENST00000614337.4:n.1839T>C
NM_144508.4:c.1523T>C NP_653091.3:p.Ile508Thr
NM_170589.4:c.1601T>C NP_733468.3:p.Ile534Thr
XM_011521816.1:c.1199T>C XP_011520118.1:p.Ile400Thr
XM_011521817.1:c.1523T>C XP_011520119.1:p.Ile508Thr
XM_017022432.1:c.1199T>C XP_016877921.1:p.Ile400Thr
NM_144508.5:c.1523T>C MANE Select NP_653091.3:p.Ile508Thr
NM_170589.5:c.1601T>C NP_733468.3:p.Ile534Thr