Canonical Allele Identifier: CA2171877535
Gene: KNL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651629_40651633delinsAAACC , CM000677.2:g.40651629_40651633delinsAAACC GRCh38
NC_000015.9:g.40943827_40943831delinsAAACC , CM000677.1:g.40943827_40943831delinsAAACC GRCh37
NC_000015.8:g.38731119_38731123delinsAAACC NCBI36
NG_033114.1:g.62381_62385delinsAAACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6314+57_6314+61delinsAAACC MANE Select ENSP00000382576.3:n.6314+57_6314+61delinsAAACC
ENST00000346991.9:c.6392+57_6392+61delinsAAACC ENSP00000335463.6:n.6392+57_6392+61delinsAAACC
ENST00000399668.6:c.6314+57_6314+61delinsAAACC ENSP00000382576.2:n.6314+57_6314+61delinsAAACC
ENST00000526913.5:c.3447+57_3447+61delinsAAACC
ENST00000532347.1:n.394+57_394+61delinsAAACC
NM_144508.4:c.6314+57_6314+61delinsAAACC NP_653091.3:n.6314+57_6314+61delinsAAACC
NM_170589.4:c.6392+57_6392+61delinsAAACC NP_733468.3:n.6392+57_6392+61delinsAAACC
XM_011521816.1:c.5990+57_5990+61delinsAAACC XP_011520118.1:n.5990+57_5990+61delinsAAACC
XM_011521817.1:c.6314+57_6314+61delinsAAACC XP_011520119.1:n.6314+57_6314+61delinsAAACC
XM_017022432.1:c.5990+57_5990+61delinsAAACC XP_016877921.1:n.5990+57_5990+61delinsAAACC
NM_144508.5:c.6314+57_6314+61delinsAAACC MANE Select NP_653091.3:n.6314+57_6314+61delinsAAACC
NM_170589.5:c.6392+57_6392+61delinsAAACC NP_733468.3:n.6392+57_6392+61delinsAAACC