Canonical Allele Identifier: CA2171877463
Gene: KNL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651457_40651458delinsGC , CM000677.2:g.40651457_40651458delinsGC GRCh38
NC_000015.9:g.40943655_40943656delinsGC , CM000677.1:g.40943655_40943656delinsGC GRCh37
NC_000015.8:g.38730947_38730948delinsGC NCBI36
NG_033114.1:g.62209_62210delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6213-14_6213-13delinsGC MANE Select ENSP00000382576.3:n.6213-14_6213-13delinsGC
ENST00000346991.9:c.6291-14_6291-13delinsGC ENSP00000335463.6:n.6291-14_6291-13delinsGC
ENST00000399668.6:c.6213-14_6213-13delinsGC ENSP00000382576.2:n.6213-14_6213-13delinsGC
ENST00000526913.5:c.3346-14_3346-13delinsGC
ENST00000532347.1:n.293-14_293-13delinsGC
NM_144508.4:c.6213-14_6213-13delinsGC NP_653091.3:n.6213-14_6213-13delinsGC
NM_170589.4:c.6291-14_6291-13delinsGC NP_733468.3:n.6291-14_6291-13delinsGC
XM_011521816.1:c.5889-14_5889-13delinsGC XP_011520118.1:n.5889-14_5889-13delinsGC
XM_011521817.1:c.6213-14_6213-13delinsGC XP_011520119.1:n.6213-14_6213-13delinsGC
XM_017022432.1:c.5889-14_5889-13delinsGC XP_016877921.1:n.5889-14_5889-13delinsGC
NM_144508.5:c.6213-14_6213-13delinsGC MANE Select NP_653091.3:n.6213-14_6213-13delinsGC
NM_170589.5:c.6291-14_6291-13delinsGC NP_733468.3:n.6291-14_6291-13delinsGC